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Human Genome Region REGION39

Assembly:
GRCh38.p14
Location:
chr19:22,120,850-22,300,666
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 ALT Unavailable Unavailable Unavailable
           

REGION39 -- chr19 (CM000681.2):22,120,850-22,300,666