A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583524



Internal ID16370933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163202886..163281796hg38UCSC Ensembl
Innerchr2:164059396..164138306hg19UCSC Ensembl
Innerchr2:163767642..163846552hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3878911
hg1978911
hg1878911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv924940
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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