LIST OF DYS MARKERS

The following DYS (DNA Y-chromosome Segment) markers are commonly used in genealogical DNA testing.
DYS454 is the least varying Y-STR marker, and multi-copy marker DYS464 is the most varying Y-STR marker.
The location on the Y chromosome of numbered DYS markers can be roughly given with cytogenetic localization. For example DYS449 is located at Yp11.2 - meaning the Y chromosome, petit arm, band 1, sub-band 1, sub-sub-band 2 - DYS449[1].

Contents
Mutation rates
DYS markers
Notes & References
See also
External links

Mutation rates


Mutation rates are those per generation, as estimated in Chandler (2006)[2]. The quoted estimated errors are typically +/- 15-20%. Alternative estimates from observed pedigrees are also available for some markers [3].
It appears that some trinucleotide markers may have much higher mutation rates at some repeat lengths than at others. For example, variation of the trinucleotide DYS 388 is generally very slow in most haplogroups, when it takes the values 11-13. But there appears to be much greater variation and more rapid mutation in Haplogroup J, where it typically has values 14-18. Similarly the trinucleotide DYS 392 is reported to be "fast" in haplogroups N and Q, where it takes values 14-16 which are rare in other groups. [4].

DYS markers


DYS#notesDNA sequence repeat motifallelesmutation ratelinks
DYS19''see DYS394''
DYS385DYS385 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.GAAA7 - 280.00226NIST fact sheet
DYS388ATT10-160.00022 [5]
DYS389DYS389 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:9-17ii:24-340.00186, 0.00242NIST fact sheet
DYS390(TCTA) (TCTG)17-280.00311NIST fact sheet
DYS391TCTA6-140.00265NIST fact sheet
DYS392TAT6-170.00052 5NIST fact sheet
DYS393DYS393 is also known as 'DYS395'.AGAT9-170.00076NIST fact sheet
DYS394DYS394 is also known as 'DYS19'.TAGA10-190.00151NIST fact sheet
DYS413Found in the Palindromic region of the Y DNA
DYS425DYS425 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.TGT10-155
DYS426GTT10-120.00009 5NIST fact sheet
DYS434TAAT (CTAT)9-12NIST fact sheet
DYS435TGGA9-13
DYS436GTT9-155
DYS437TCTA13-170.00099NIST fact sheet
DYS438TTTTC6-140.00055NIST fact sheet
DYS439DYS439 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.AGAT9-140.00477NIST fact sheet
DYS441CCTT12-18A novel multiplex PCR system
DYS442TATC10-140.00324A novel multiplex PCR system
DYS443TTCC12-17
DYS444TAGA11-15A novel multiplex PCR system
DYS445TTTA10-13A novel multiplex PCR system
DYS446TCTCT10-18Sorenson Marker Details
DYS447TAA'W'A22-290.00264NIST fact sheet
DYS448AGAGAT20-260.00135NIST fact sheet
DYS449TTTC26-360.00838Sorenson Marker Details
GDB fact sheet
DYS450TTTTA8-11
DYS452'Y'ATAC27-33
DYS453AAAT9-13
DYS454DYS454 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).AAAT10-120.00016
DYS455AAAT8-120.00016Sorenson Marker Details
DYS456AGAT13-180.00735Sorenson Marker Details
DYS458GAAA13-200.00814Sorenson Marker Details
DYS459This is a multi-copy marker, and includes DYS459a and DYS459b.TAAA7-100.00132
DYS460DYS460 was originally known as Y-GATA-A7.1.ATAG7-120.00402NIST fact sheet
DYS461DYS461 was originally known as Y-GATA-A7.2.(TAGA) CAGA8-14NIST fact sheet
DYS462TATG8-14
DYS463AA'R'GG18-27GDB fact sheet
DYS464DYS464 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 DNACCTT9-200.00566Forensic value of the multicopy Y-STR marker DYS464
DYS464X testing
DYS464 discrepancies
DYS481CTT20-305
DYS485TTA10-185
DYS487ATT12-145
DYS490TTA12-165
DYS494TAT105
DYS495AAT12-185
DYS497TAT13-165
DYS504
DYS505TCCT9-15
DYS508TATC8-15
DYS520ATA'S'18-26
DYS522GATA8-17
DYS525TAGA9-12
DYS531AAAT11-13
DYS532CTTT9-17
DYS533ATCT9-14
DYS534CTTT10-20
DYS540TTAT10-13
DYS549AGAT10-14
DYS556AATA8-12
DYS557TTTC
DYS565TAAA9-14
DYS570TTTC12-230.00790GDB fact sheet
DYS572AAAT8-12
DYS573TTTA8-11
DYS575AAAT8-12
DYS576AAAG13-210.01022
DYS578AAAT7-10
DYS589TTATT13
DYS594TAAAA8-11
DYS607AAGG8-200.00411
DYS612
DYS614
DYS626AAAG
DYS632CATT
DYS635Also known as 'Y-GATA-C4'T'S'TA compound17-27
DYS636
DYS638TTTA10-12
DYS641TAAA7-11
DYS643CTTTT7-15
DYS714
DYS716
DYS717
DYS724Palindromic; also known as 'CDY'0.03531GDB Fact Sheet
DYS725Palindromic
DYS726YSTR marker in the pericentromeric region.11-16
DYF371DYF371 is a multicopy, palindromic region marker. Includes the DYS425 marker & can be informative in cases of null values at that marker.
DYF385S1Duplicated YSTR marker in close proximity to DYS4599-12
DYF397DYF397 is a palindromic region marker.
DYF399S1An 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
DYF401DYF401 is a palindromic region marker.
DYF406S1
DYF408DYF408 is a palindromic region marker.
DYF411DYF411 is a palindromic region marker.
DXYS156
YCAIIYCAII is a multi-copy marker which includes YCAIIa & YCAIIb0.00123
Y-GATA-H4TAGA8-13 (25-30)0.00208NIST fact sheet
Y-GATA-C4''see DYS635''
Y-GATA-A10TAGA13-18NIST fact sheet
Y-GGAAT-1B07

Notes & References


1. DYS449 in the GDB Human Genome Database
2. Chandler (2006) (but see also this mailing list discussion )
3. YHRD mutation rates
4. GENEALOGY-DNA-L Archives — DYS 388 Mutation Rate?
5. Trinucleotide - see #Mutation rates


★ Kayser et al (2004), A Comprehensive Survey of Human Y-Chromosomal Microsatellites Am. J. Hum. Genet., '74' 1183-1197. NB online only data file

See also



List of binary polymorphisms

List of DXS markers

External links



Y STR fact sheet

Y-DNA Testing Company STR Marker Comparison Chart

SMGF Y Marker Details

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