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Human Genome Region REGION38

Assembly:
GRCh38.p14
Location:
chr19:34,152,260-34,300,950
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383574.1 NW_003315963.1 ALT Unavailable Unavailable Unavailable
           

REGION38 -- chr19 (CM000681.2):34,152,260-34,300,950