A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517298



Internal ID15444591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112709854..112716149hg38UCSC Ensembl
Innerchr11:112580577..112586872hg19UCSC Ensembl
Innerchr11:112085787..112092082hg18UCSC Ensembl
Innerchr11:112085787..112092082hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg386296
hg196296
hg186296
hg176296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654237, nssv667492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517298
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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