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Human Genome Region REGION184

Assembly:
GRCh38.p11
Location:
chr22:23,354,043-23,516,062
Cytogenetic location:

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No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270878.1 NT_187632.1 ALT 186,262 198 24,390
           

REGION184 -- chr22 (NC_000022.11):23,354,043-23,516,062