A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589245



Internal ID16029968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72450..170062hg38UCSC Ensembl
Innerchr3:114133..211745hg19UCSC Ensembl
Innerchr3:89133..186745hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3897613
hg1997613
hg1897613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8144n54
Supporting Variantsnssv1152228
SamplesHGDP00459
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589245
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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