A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152462



Internal ID15507065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4140066..4271051hg38UCSC Ensembl
Innerchr3:4181750..4312735hg19UCSC Ensembl
Innerchr3:4156750..4287735hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38130986
hg19130986
hg18130986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589442
Supporting Variants
Samples1780854417_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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