A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596941



Internal ID16384350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5511877..5636345hg38UCSC Ensembl
Innerchr5:5511990..5636458hg19UCSC Ensembl
Innerchr5:5564990..5689458hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38124469
hg19124469
hg18124469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9552n54
Supporting Variantsnssv1023696
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596941
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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