A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586081



Internal ID16026804
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 StatusM
Merged Variants
Supporting Variantsnssv940716
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)nsv586081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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