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Human Genome Region REGION292

Assembly:
GRCh38.p14
Location:
chr22:16,124,788-16,489,297
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
ML143378.1 NW_021160024.1 FIX Unavailable Unavailable Unavailable
           

REGION292 -- chr22 (CM000684.2):16,124,788-16,489,297