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Human Genome Region REGION42

Assembly:
GRCh37.p13
Location:
chr21:23,474,793-23,669,288
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383579.1 NW_003315968.1 NOVEL 201,198 48 6,718
           

REGION42 -- chr21 (NC_000021.8):23,474,793-23,669,288