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Human Genome Region REGION8

Assembly:
GRCh37.p11
Location:
chr5:161,800,673-161,968,654
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1155 Resolved NOVEL patch GL383531.1 created to capture sequence from AC207995.2 not represented in reference chromosome AC207995.2, which represents a sequence variant to GRCh37 by containing 5480bp more than component AC091996.3, has been uploaded to the Chr. 5 Alt-Ref-Loci TPF
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383531.1 NW_003315919.1 NOVEL 173,459 64 5,503
           

REGION8 -- chr5 (NC_000005.9):161,800,673-161,968,654