A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586473



Internal ID16373882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62065106..62066675hg38UCSC Ensembl
Innerchr20:60640162..60641731hg19UCSC Ensembl
Innerchr20:60073557..60075126hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381570
hg191570
hg181570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7647n54
Supporting Variantsnssv942036
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586473
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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