A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785116



Internal ID15732386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131680956..131681565hg38UCSC Ensembl
Innerchr11:131550850..131551459hg19UCSC Ensembl
Innerchr11:131056060..131056669hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38610
hg19610
hg18610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556577
Supporting Variants
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785116
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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