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Human Genome Region REGION26

Assembly:
GRCh37.p13
Location:
chr16:55,822,434-56,002,460
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383556.1 NW_003315945.1 NOVEL 192,462 227 12,772
           

REGION26 -- chr16 (NC_000016.9):55,822,434-56,002,460