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Human Genome Region ZNF66

Assembly:
GRCh37.p10
Location:
chr19:20,845,947-21,225,187
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1186 Resolved NOVEL patch GL383573.1 created to capture sequence from AC008463.7 not represented in reference chromosome AC008463.7, which represents a sequence variant to GRCh37 by containing 6471bp more than Reference components AC008739.5 and AC008739.5, has been uploaded 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
GL383573.1 NW_003315962.1 NOVEL 385,657 1,093 7,153
           

ZNF66 -- chr19 (NC_000019.9):20,845,947-21,225,187