A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962382



Internal ID15909652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39146691..39189506hg38UCSC Ensembl
Innerchr3:39188182..39230997hg19UCSC Ensembl
Innerchr3:39163186..39206001hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3842816
hg1942816
hg1842816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590104
Supporting Variants
Samples
Known GenesCSRNP1, XIRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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