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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29 mapped markers found:

1788chromosome 20:10287794-10287873
AL034503chromosome 20:10423636-10423820
BV727904chromosome 20:10444973-10445366
D20S504chromosome 20:10063671-10063928
D20S729chromosome 20:10091418-10091681
D20S763chromosome 20:10286842-10287016
D9S914chromosome 20:10374760-10374991
G60203chromosome 20:10385924-10386256
MARC_11717-11718:1029180244:1chromosome 20:10287208-10287551
MKKS__7396chromosome 20:10385810-10386305
RH102299chromosome 20:10298615-10298791
RH122608chromosome 20:10275203-10275545
RH123884chromosome 20:10351459-10351734
RH28686chromosome 20:10278428-10278510
RH46023chromosome 20:10385963-10386097
RH47511chromosome 20:10278481-10278579
RH64137chromosome 20:10287734-10287832
SHGC-107163chromosome 20:10311058-10311255
SHGC-12843chromosome 20:10286857-10287058
SHGC-145770chromosome 20:10165766-10166103
SHGC-68771chromosome 20:10202347-10202570
SHGC-79896chromosome 20:10429990-10430205
STS-AA017039chromosome 20:10287759-1028788310287798-10288010
STS-R67339chromosome 20:10394155-10394294
WI-14216chromosome 20:10271152-10271302
WI-18780chromosome 20:10286871-10286999
WI-19889chromosome 20:10278278-10278452
Z94390chromosome 20:10194363-10194482
Z94685chromosome 20:10241851-10242040