A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586466



Internal ID16373875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064684..62066551hg38UCSC Ensembl
Innerchr20:60639740..60641607hg19UCSC Ensembl
Innerchr20:60073135..60075002hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381868
hg191868
hg181868
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7646n54
Supporting Variantsnssv942027, nssv942026, nssv942028
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586466
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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