A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583252



Internal ID16370661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145972341..146036056hg38UCSC Ensembl
Innerchr2:146729909..146793624hg19UCSC Ensembl
Innerchr2:146446379..146510094hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3863716
hg1963716
hg1863716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7097n54
Supporting Variantsnssv920284
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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