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Human Genome Region REGION79

Assembly:
GRCh37.p10
Location:
chr1:235,167,042-235,192,211
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1473 Resolved There is a gap in the assembly between components CR589906.2 and BX470108.3 originally described in HG-541. An extension into this gap from the left side is being considered for patch release. There is a gap in the assembly between components CR589906.2 and BX470108.3 originally described in HG-541. An extension into this gap from the left side is being considered for patch release.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806575.1 NW_004070865.1 FIX 47,409 0 22,239
           

REGION79 -- chr1 (NC_000001.10):235,167,042-235,192,211