A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv924943



Internal ID16218899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163492069..163551804hg38UCSC Ensembl
Innerchr2:164348579..164408314hg19UCSC Ensembl
Innerchr2:164056825..164116560hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3859736
hg1959736
hg1859736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583528
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)nssv924943
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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