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Human Genome Region GPI

Assembly:
GRCh38.p9
Location:
chr19:34,350,807-34,392,977
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270866.1 NT_187619.1 ALT 43,156 330 1,037
           

GPI -- chr19 (NC_000019.10):34,350,807-34,392,977