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Human Genome Region REGION2

Assembly:
GRCh37.p13
Location:
chr1:153,673,007-153,838,214
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383518.1 NW_003315905.1 NOVEL 182,439 49 17,291
           

REGION2 -- chr1 (NC_000001.10):153,673,007-153,838,214