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Human Genome Region REGION222

Assembly:
GRCh38.p14
Location:
chr4:14,931,450-15,019,028
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KQ090013.1 NW_013171799.1 NOVEL Unavailable Unavailable Unavailable
           

REGION222 -- chr4 (CM000666.2):14,931,450-15,019,028