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Human Genome Region WILLIAMS

Assembly:
GRCh37.p11
Location:
chr7:71,935,722-75,921,852
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1257 Resolved Repetitive structure and mixed libraries in the Williams region result in a possible lack of representation of a true haplotype and a recalcitrant gap. CH17 clones have been sequenced in the duplicated regions of the Williams Region and replace the clones from mixed haplotypes in these two locations: between AC091738.4 - AC005049.2 and between AC004851.2 - AC004491.2.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH159134.2 NW_003871064.1 FIX 3,821,770 2,082 60,921
           

WILLIAMS -- chr7 (NC_000007.13):71,935,722-75,921,852