A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586080



Internal ID16373489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45573240..45578612hg38UCSC Ensembl
Innerchr20:44201879..44207251hg19UCSC Ensembl
Innerchr20:43635293..43640665hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385373
hg195373
hg185373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940715
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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