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Human Genome Region REGION293

Assembly:
GRCh38.p14
Location:
chr22:49,970,785-49,983,074
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
ML143379.1 NW_021160025.1 FIX Unavailable Unavailable Unavailable
           

REGION293 -- chr22 (CM000684.2):49,970,785-49,983,074