A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763569



Internal ID15710839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:823590..843713hg38UCSC Ensembl
Innerchr11:823590..843713hg19UCSC Ensembl
Innerchr11:813590..833713hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3820124
hg1920124
hg1820124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552874
Supporting Variants
Samples
Known GenesCD151, EFCAB4A, PNPLA2, POLR2L, TSPAN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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