A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591359



Internal ID16378768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119024001..119083007hg38UCSC Ensembl
Innerchr3:118742848..118801854hg19UCSC Ensembl
Innerchr3:120225538..120284544hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3859007
hg1959007
hg1859007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8516n54
Supporting Variantsnssv971659, nssv971658
Samples
Known GenesIGSF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591359
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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