A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584071



Internal ID16371480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192681272..192740517hg38UCSC Ensembl
Innerchr2:193545998..193605243hg19UCSC Ensembl
Innerchr2:193254243..193313488hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3859246
hg1959246
hg1859246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928437
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584071
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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