A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943743



Internal ID16237699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63217271..63268953hg38UCSC Ensembl
Innerchr20:61848623..61900305hg19UCSC Ensembl
Innerchr20:61319068..61370750hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3851683
hg1951683
hg1851683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586562
Supporting Variants
Samples
Known GenesBIRC7, FLJ16779, MIR3196, NKAIN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943743
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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