DYS#
| notes
| DNA sequence repeat motif
| alleles
| mutation rate
| links
|
DYS19
| see DYS394
| —
| —
| —
| —
|
DYS385
| DYS385 is a multi-copy marker, and includes DYS385a and DYS385b. The order of DYS385a and DYS385b may be reversed, their sequence is referred to as the Kittler order.
| GAAA
| 7 - 28
| 0.00226
| NIST fact sheet
|
DYS388
|
| ATT
| 10-16
| 0.00022 [5]
|
|
DYS389
| DYS389 is a multi-copy marker, and includes DYS389i and DYS389ii. DYS389ii refers to the total length of DYS389. Therefore, when there is a one step mutation at DYS389i, it will also appear in DYS389ii.
| (TCTG) (TCTA) (TCTG) (TCTA)
| i:9-17
ii:24-34
| 0.00186, 0.00242
| NIST fact sheet
|
DYS390
|
| (TCTA) (TCTG)
| 17-28
| 0.00311
| NIST fact sheet
|
DYS391
|
| TCTA
| 6-14
| 0.00265
| NIST fact sheet
|
DYS392
|
| TAT
| 6-17
| 0.00052 [5]
| NIST fact sheet
|
DYS393
| DYS393 is also known as DYS395.
| AGAT
| 9-17
| 0.00076
| NIST fact sheet
|
DYS394
| DYS394 is also known as DYS19.
| TAGA
| 10-19
| 0.00151
| NIST fact sheet
|
DYS413
| Found in the Palindromic region of the Y DNA
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DYS425
| DYS425 is associated with the defining SNP for haplogroup I1b2a1, as the SNP M284 can render a null value at this marker. It is also commonly a place of occurrence for a recLOH which can render a null value.
| TGT
| 10-15
| [5]
|
|
DYS426
|
| GTT
| 10-12
| 0.00009 [5]
| NIST fact sheet
|
DYS434
|
| TAAT (CTAT)
| 9-12
|
| NIST fact sheet
|
DYS435
|
| TGGA
| 9-13
|
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DYS436
|
| GTT
| 9-15
| [5]
|
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DYS437
|
| TCTA
| 13-17
| 0.00099
| NIST fact sheet
|
DYS438
|
| TTTTC
| 6-14
| 0.00055
| NIST fact sheet
|
DYS439
| DYS439 is also known as Y-GATA-A4. DYS439 is associated with the defining SNP for haplogroup R1b1c9a, as the SNP can render a null value at this marker.
| AGAT
| 9-14
| 0.00477
| NIST fact sheet
|
DYS441
|
| CCTT
| 12-18
|
| A novel multiplex PCR system
|
DYS442
|
| TATC
| 10-14
| 0.00324
| A novel multiplex PCR system
|
DYS443
|
| TTCC
| 12-17
|
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DYS444
|
| TAGA
| 11-15
|
| A novel multiplex PCR system
|
DYS445
|
| TTTA
| 10-13
|
| A novel multiplex PCR system
|
DYS446
|
| TCTCT
| 10-18
|
| Sorenson Marker Details
|
DYS447
|
| TAAWA
| 22-29
| 0.00264
| NIST fact sheet
|
DYS448
|
| AGAGAT
| 20-26
| 0.00135
| NIST fact sheet
|
DYS449
|
| TTTC
| 26-36
| 0.00838
| Sorenson Marker Details
GDB fact sheet
|
DYS450
|
| TTTTA
| 8-11
|
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DYS452
|
| YATAC
| 27-33
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DYS453
|
| AAAT
| 9-13
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DYS454
| DYS454 is the least varying Y-STR marker commonly used in genealogical DNA testing. Of the entries for DYS454 at Ybase, 96% have 11 repeats, 3% have 10 repeats, and 2% have 12 repeats (source).
| AAAT
| 10-12
| 0.00016
|
|
DYS455
|
| AAAT
| 8-12
| 0.00016
| Sorenson Marker Details
|
DYS456
|
| AGAT
| 13-18
| 0.00735
| Sorenson Marker Details
|
DYS458
|
| GAAA
| 13-20
| 0.00814
| Sorenson Marker Details
|
DYS459
| This is a multi-copy marker, and includes DYS459a and DYS459b.
| TAAA
| 7-10
| 0.00132
|
|
DYS460
| DYS460 was originally known as Y-GATA-A7.1.
| ATAG
| 7-12
| 0.00402
| NIST fact sheet
|
DYS461
| DYS461 was originally known as Y-GATA-A7.2.
| (TAGA) CAGA
| 8-14
|
| NIST fact sheet
|
DYS462
|
| TATG
| 8-14
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DYS463
|
| AARGG
| 18-27
|
| GDB fact sheet
|
DYS464
| DYS464 is a multi-copy marker, and includes DYS464a, DYS464b, DYS464c, and DYS464d. Rarely it can also include DYS464e, DYS464f, and DYS464g. DYS464 is the most varying Y-STR marker (source). This marker can also be typed with separate g-types and c-types to increase resolution. The type variance is based on a SNP that can be found in most R1b haplogroup males. It is part of the Palindromic region of Y DNA
| CCTT
| 9-20
| 0.00566
| Forensic value of the multicopy Y-STR marker DYS464
DYS464X testing
DYS464 discrepancies
|
DYS481
|
| CTT
| 20-30
| [5]
|
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DYS485
|
| TTA
| 10-18
| [5]
|
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DYS487
|
| ATT
| 12-14
| [5]
|
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DYS490
|
| TTA
| 12-16
| [5]
|
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DYS494
|
| TAT
| 10
| [5]
|
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DYS495
|
| AAT
| 12-18
| [5]
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DYS497
|
| TAT
| 13-16
| [5]
|
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DYS504
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DYS505
|
| TCCT
| 9-15
|
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DYS508
|
| TATC
| 8-15
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DYS520
|
| ATAS
| 18-26
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DYS522
|
| GATA
| 8-17
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DYS525
|
| TAGA
| 9-12
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DYS531
|
| AAAT
| 11-13
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DYS532
|
| CTTT
| 9-17
|
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DYS533
|
| ATCT
| 9-14
|
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DYS534
|
| CTTT
| 10-20
|
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DYS540
|
| TTAT
| 10-13
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DYS549
|
| AGAT
| 10-14
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DYS556
|
| AATA
| 8-12
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DYS557
|
| TTTC
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DYS565
|
| TAAA
| 9-14
|
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DYS570
|
| TTTC
| 12-23
| 0.00790
| GDB fact sheet
|
DYS572
|
| AAAT
| 8-12
|
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DYS573
|
| TTTA
| 8-11
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DYS575
|
| AAAT
| 8-12
|
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DYS576
|
| AAAG
| 13-21
| 0.01022
|
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DYS578
|
| AAAT
| 7-10
|
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DYS589
|
| TTATT
| 13
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DYS594
|
| TAAAA
| 8-11
|
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DYS607
|
| AAGG
| 8-20
| 0.00411
|
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DYS612
|
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DYS614
|
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DYS626
|
| AAAG
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DYS632
|
| CATT
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DYS635
| Also known as Y-GATA-C4
| TSTA compound
| 17-27
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DYS636
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DYS638
|
| TTTA
| 10-12
|
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DYS641
|
| TAAA
| 7-11
|
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DYS643
|
| CTTTT
| 7-15
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DYS714
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DYS716
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DYS717
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DYS724
| Palindromic; also known as CDY
|
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| 0.03531
| GDB Fact Sheet
|
DYS725
| Palindromic
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DYS726
| YSTR marker in the pericentromeric region.
|
| 11-16
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DYF371
| DYF371 is a multicopy, palindromic region marker. Includes the DYS425 marker & can be informative in cases of null values at that marker.
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DYF385S1
| Duplicated YSTR marker in close proximity to DYS459
|
| 9-12
|
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DYF397
| DYF397 is a palindromic region marker.
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DYF399
| An asymmetric three allele STR locus that can be used to observe deletions and recombinational rearrangements in the palindromic region of the Y chromosome.
|
| 17-29 (many incomplete alleles)
|
| nomenclature
|
DYF401
| DYF401 is a palindromic region marker.
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DYF406S1
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DYF408
| DYF408 is a palindromic region marker.
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DYF411
| DYF411 is a palindromic region marker.
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DXYS156
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YCAII
| YCAII is a multi-copy marker which includes YCAIIa & YCAIIb
|
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| 0.00123
|
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Y-GATA-H4
|
| TAGA
| 8-13 (25-30)
| 0.00208
| NIST fact sheet
|
Y-GATA-C4
| see DYS635
| —
| —
| —
| —
|
Y-GATA-A10
|
| TAGA
| 13-18
|
| NIST fact sheet
|
Y-GGAAT-1B07
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