A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962535



Internal ID15909805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46754860..46811189hg38UCSC Ensembl
Innerchr3:46796350..46852679hg19UCSC Ensembl
Innerchr3:46771354..46827683hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3856330
hg1956330
hg1856330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590183
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)nssv962535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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