A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942026



Internal ID16235982
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586466
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)nssv942026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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