A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv767782



Internal ID15715052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9646281..9806324hg38UCSC Ensembl
Innerchr11:9667828..9827871hg19UCSC Ensembl
Innerchr11:9624404..9784447hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38160044
hg19160044
hg18160044
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553468
Supporting Variants
Samples
Known GenesLOC440028, SBF2, SBF2-AS1, SWAP70
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv767782
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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