A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519489



Internal ID15446782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127300878..127318613hg38UCSC Ensembl
Innerchr11:127170773..127188508hg19UCSC Ensembl
Innerchr11:126675983..126693718hg18UCSC Ensembl
Innerchr11:126675983..126693718hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3817736
hg1917736
hg1817736
hg1717736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696879
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519489
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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