Human (GRCh37.p13)

Assembly exceptions

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

URL to turn this track on

Copy the above url to force this track to be turned on

Click on the star to add/remove this track from your favourites

Click on the cross to turn the track off

Click to highlight/unhighlight this track

Assembly exceptions

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

URL to turn this track on

Copy the above url to force this track to be turned on

Click on the star to add/remove this track from your favourites

Click on the cross to turn the track off

Click to highlight/unhighlight this track

10 mapped markers found:

A008N41chromosome 19:33872165-33872453
D19S1116chromosome 19:33870862-33871002
D19S658Echromosome 19:33873385-33873515
D19S695Echromosome 19:33870882-33870981
D19S722chromosome 19:33873342-33873467
RH18013chromosome 19:33870586-33870728
RH79127chromosome 19:33870653-33870830
RH91734chromosome 19:33873343-33873465
SHGC-35371chromosome 19:33870608-33870830
STS-T83376chromosome 19:33866485-33866651