A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586461



Internal ID16373870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064568..62066261hg38UCSC Ensembl
Innerchr20:60639624..60641317hg19UCSC Ensembl
Innerchr20:60073019..60074712hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381694
hg191694
hg181694
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7646n54
Supporting Variantsnssv942008, nssv942005, nssv942007, nssv942006
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586461
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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