A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583556



Internal ID16370965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:164973878..164985892hg38UCSC Ensembl
Innerchr2:165830388..165842402hg19UCSC Ensembl
Innerchr2:165538634..165550648hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3812015
hg1912015
hg1812015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583556
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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