Human (GRCh37.p13)

Assembly exceptions

GRC assembly patches, haplotype (HAPs) and pseudo autosomal regions (PARs)

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Assembly exceptions

GRC assembly patches, haplotype (HAPs) and pseudo autosomal regions (PARs)

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46 mapped markers found:

AGRN__4265chromosome 1:990830-991514
AL033601chromosome 1:721333-721464
D1S2217chromosome 1:797159-797557
D1S2336Echromosome 1:982963-983061
D1S282Echromosome 1:987636-987732
ECD03212chromosome 1:14421-15222
G22229chromosome 1:780386-780535
G62009chromosome 1:949574-949696
GDB:229298chromosome 1:49786-49915
L28277chromosome 1:559430-559611
PMC109173P1chromosome 1:568034-568913
PMC113853P1chromosome 1:565031-566006
PMC135632P2chromosome 1:949396-949694
PMC196577P3chromosome 1:568112-568534
PMC20756P1chromosome 1:568034-568121
PMC20756P2chromosome 1:568034-568932
PMC20756P3chromosome 1:567676-568223
PMC55343P1chromosome 1:564739-565363
PMC55343P2chromosome 1:566868-567469
PMC55343P3chromosome 1:567909-568488
PMC55343P4chromosome 1:568829-568915
PMC55343P5chromosome 1:568829-569431
PMC55343P6chromosome 1:569328-569431
PMC55343P7chromosome 1:569328-569965
PMC84353P2chromosome 1:949396-949632
REN94416chromosome 1:12722-12949
RH103110chromosome 1:900869-901011
RH25952chromosome 1:794585-794695
RH37561chromosome 1:764485-764697
RH65042chromosome 1:746384-746486
RH66043chromosome 1:730669-730797
RH66824chromosome 1:949680-949816
RH80369chromosome 1:949677-949917
RH80426chromosome 1:991247-991490
RH98513chromosome 1:567937-568064
SHGC-145224chromosome 1:780959-781260
SHGC-145703chromosome 1:863980-864268
SHGC-145870chromosome 1:853731-854066
SHGC-146656chromosome 1:873260-873546
SHGC-146903chromosome 1:900426-900775
SHGC-30399chromosome 1:723203-723330
SHGC-74080chromosome 1:878944-879152
SHGC-74081chromosome 1:991113-991233
SHGC-74122chromosome 1:879613-879744
SHGC-74128chromosome 1:949571-949695
sY1688chromosome 1:723660-724192