A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590147



Internal ID16030870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42248596..42310311hg38UCSC Ensembl
Innerchr3:42290088..42351803hg19UCSC Ensembl
Innerchr3:42265092..42326807hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3861716
hg1961716
hg1861716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962432
Samples
Known GenesCCK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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