A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962579



Internal ID16256535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46756643..46789244hg38UCSC Ensembl
Innerchr3:46798133..46830734hg19UCSC Ensembl
Innerchr3:46773137..46805738hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3832602
hg1932602
hg1832602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590198
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)nssv962579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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