A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785206



Internal ID16079162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134532717..134837541hg38UCSC Ensembl
Innerchr11:134402611..134707435hg19UCSC Ensembl
Innerchr11:133907821..134212645hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38304825
hg19304825
hg18304825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556656
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785206
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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