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Human Genome Region GALNT9

Assembly:
GRCh37.p10
Location:
chr12:132,806,993-132,967,794
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-996 Resolved There is an assembly gap between AC145426.6 and AC148477.3 . A 10kb extension into this gap since GRCh37 has been released as a FIX patch to GRCh37: GL383548.1.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383548.1 NW_003315937.1 FIX 165,247 162 10,212
           

GALNT9 -- chr12 (NC_000012.11):132,806,993-132,967,794