A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519192



Internal ID15099799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112160901..112193416hg38UCSC Ensembl
Innerchr11:112031624..112064139hg19UCSC Ensembl
Innerchr11:111536834..111569349hg18UCSC Ensembl
Innerchr11:111536834..111569349hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3832516
hg1932516
hg1832516
hg1732516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696675
Samples
Known GenesBCO2, IL18, TEX12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519192
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer