A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv900965



Internal ID16194921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51946390..52016355hg38UCSC Ensembl
Innerchr19:52449643..52519608hg19UCSC Ensembl
Innerchr19:57141455..57211420hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3869966
hg1969966
hg1869966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580006
Supporting Variants
Samples
Known GenesHCCAT3, ZNF350, ZNF614, ZNF615
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv900965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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