A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962397



Internal ID16256353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41318043..41691841hg38UCSC Ensembl
Innerchr3:41359534..41733333hg19UCSC Ensembl
Innerchr3:41334538..41708337hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38373799
hg19373800
hg18373800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590119
Supporting Variants
Samples
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962397
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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