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Human Genome Region REGION39

Assembly:
GRCh37.p13
Location:
chr19:22,303,652-22,483,468
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383576.1 NW_003315965.1 NOVEL 188,024 64 8,244
           

REGION39 -- chr19 (NC_000019.9):22,303,652-22,483,468