A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958052



Internal ID15905322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4762316..4797135hg38UCSC Ensembl
Innerchr3:4804000..4838819hg19UCSC Ensembl
Innerchr3:4779000..4813819hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3834820
hg1934820
hg1834820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589456
Supporting Variants
Samples
Known GenesITPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958052
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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