A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940716



Internal ID15887986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45573240..45747557hg38UCSC Ensembl
Innerchr20:44201879..44376196hg19UCSC Ensembl
Innerchr20:43635293..43809603hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38174318
hg19174318
hg18174311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586081
Supporting Variants
Samples
Known GenesSPINT4, WFDC10A, WFDC10B, WFDC11, WFDC13, WFDC8, WFDC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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