A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801431



Internal ID18830661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56994803..57244140hg38UCSC Ensembl
Innerchr19:57506171..57755508hg19UCSC Ensembl
Innerchr19:62197983..62447320hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38249338
hg19249338
hg18249338
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893256
Supporting Variants
Samples
Known GenesAURKC, DUXA, USP29, ZIM3, ZNF264, ZNF805
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=57
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801431
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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