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Human Genome Region REGION2

Assembly:
GRCh38.p14
Location:
chr1:153,700,531-153,865,738
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 ALT Unavailable Unavailable Unavailable
           

REGION2 -- chr1 (CM000663.2):153,700,531-153,865,738