A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962380



Internal ID15909650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39138418..39147352hg38UCSC Ensembl
Innerchr3:39179909..39188843hg19UCSC Ensembl
Innerchr3:39154913..39163847hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg388935
hg198935
hg188935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590102
Supporting Variants
Samples
Known GenesCSRNP1, TTC21A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962380
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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