A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962385



Internal ID16256341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39689083..39734734hg38UCSC Ensembl
Innerchr3:39730574..39776225hg19UCSC Ensembl
Innerchr3:39705578..39751229hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3845652
hg1945652
hg1845652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590108
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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