| 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 |
| 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 |
| DYS436 |
GTT |
9-15 |
[5] |
| 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 |
| 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 |
| DYS452 |
YATAC |
27-33 |
| DYS453 |
AAAT |
9-13 |
|
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 |
| 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 an 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] |
| DYS485 |
TTA |
10-18 |
[5] |
| DYS487 |
ATT |
12-14 |
[5] |
| DYS490 |
TTA |
12-16 |
[5] |
| DYS494 |
TAT |
10 |
[5] |
| DYS495 |
AAT |
12-18 |
[5] |
| DYS497 |
TAT |
13-16 |
[5] |
| DYS504 |
| DYS505 |
TCCT |
9-15 |
| DYS508 |
TATC |
8-15 |
| DYS520 |
ATAS |
18-26 |
| DYS522 |
GATA |
8-17 |
| DYS525 |
TAGA |
9-12 |
| DYS531 |
AAAT |
11-13 |
| DYS532 |
CTTT |
9-17 |
| DYS533 |
ATCT |
9-14 |
| DYS534 |
CTTT |
10-20 |
| DYS540 |
TTAT |
10-13 |
| DYS549 |
AGAT |
10-14 |
| DYS556 |
AATA |
8-12 |
| DYS557 |
TTTC |
| DYS565 |
TAAA |
9-14 |
| DYS570 |
TTTC |
12-23 |
0.00790 |
GDB fact sheet |
| DYS572 |
AAAT |
8-12 |
| DYS573 |
TTTA |
8-11 |
| DYS575 |
AAAT |
8-12 |
| DYS576 |
AAAG |
13-21 |
0.01022 |
| DYS578 |
AAAT |
7-10 |
| DYS589 |
TTATT |
13 |
| DYS594 |
TAAAA |
8-11 |
| DYS607 |
AAGG |
8-20 |
0.00411 |
| DYS612 |
| DYS614 |
| DYS626 |
AAAG |
| DYS632 |
CATT |
| DYS635 |
Also known as Y-GATA-C4 |
TSTA compound |
17-27 |
| DYS636 |
| DYS638 |
TTTA |
10-12 |
| DYS641 |
TAAA |
7-11 |
| DYS643 |
CTTTT |
7-15 |
| DYS714 |
| DYS716 |
| DYS717 |
| DYS724 |
Palindromic; also known as CDY |
0.03531 |
GDB Fact Sheet |
| DYS725 |
Palindromic |
| DYS726 |
YSTR marker in the pericentromeric region. |
11-16 |
| DYF371 |
DYF371 is a multicopy, palindromic region marker. Includes the DYS425 marker & can be informative in cases of null values at that marker. |
| DYF385S1 |
Duplicated YSTR marker in close proximity to DYS459 |
9-12 |
| DYF397 |
DYF397 is a palindromic region marker. |
|
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. |
| DYF406S1 |
| DYF408 |
DYF408 is a palindromic region marker. |
| DYF411 |
DYF411 is a palindromic region marker. |
| DXYS156 |
| YCAII |
YCAII is a multi-copy marker which includes YCAIIa & YCAIIb |
0.00123 |
| 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 |