A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590966



Internal ID16378375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89855732..90150609hg38UCSC Ensembl
Innerchr3:89904882..90199759hg19UCSC Ensembl
Innerchr3:89987572..90282449hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38294878
hg19294878
hg18294878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8438n54
Supporting Variantsnssv967750
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590966
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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