A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586464



Internal ID16373873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064568..62066675hg38UCSC Ensembl
Innerchr20:60639624..60641731hg19UCSC Ensembl
Innerchr20:60073019..60075126hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382108
hg192108
hg182108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7645n54
Supporting Variantsnssv942023, nssv942024
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586464
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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