A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893256



Internal ID18837390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56994803..57244140hg38UCSC Ensembl
Outerchr19:56994803..57244140hg38UCSC Ensembl
Innerchr19:57506171..57755508hg19UCSC Ensembl
Outerchr19:57506171..57755508hg19UCSC Ensembl
Innerchr19:62197983..62447320hg18UCSC Ensembl
Outerchr19:62197983..62447320hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38249338
hg19249338
hg18249338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801483, essv25801431
Samples
Known GenesAURKC, DUXA, USP29, ZIM3, ZNF264, ZNF805
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893256
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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