A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586452



Internal ID16373861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064345..62066033hg38UCSC Ensembl
Innerchr20:60639401..60641089hg19UCSC Ensembl
Innerchr20:60072796..60074484hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381689
hg191689
hg181689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7644n54
Supporting Variantsnssv941982
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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