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Human Genome Region REGION37

Assembly:
GRCh37.p10
Location:
chr19:21,831,092-21,991,834
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1188 Resolved NOVEL patch GL383575.1 created to capture sequence from AC226770.1 not represented in reference chromosome AC226770.1 represents a sequence variant containing approximately 9.5 kb of sequence not found in GRCh37 and it has been added to the chr 19 (alt_ref_loci_1) TPF.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383575.2 NW_003315964.2 NOVEL 170,222 107 9,527
           

REGION37 -- chr19 (NC_000019.9):21,831,092-21,991,834