A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586474



Internal ID16373883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62065214..62069722hg38UCSC Ensembl
Innerchr20:60640270..60644778hg19UCSC Ensembl
Innerchr20:60073665..60078173hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384509
hg194509
hg184509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942037
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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