A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942029



Internal ID16235985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064684..62066675hg38UCSC Ensembl
Innerchr20:60639740..60641731hg19UCSC Ensembl
Innerchr20:60073135..60075126hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381992
hg191992
hg181992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586467
Supporting Variants
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv942029
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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