A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962547



Internal ID15909817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46755146..46798800hg38UCSC Ensembl
Innerchr3:46796636..46840290hg19UCSC Ensembl
Innerchr3:46771640..46815294hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3843655
hg1943655
hg1843655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590188
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962547
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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