A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779323



Internal ID16073279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79268600..79307760hg38UCSC Ensembl
Innerchr11:78979645..79018805hg19UCSC Ensembl
Innerchr11:78657293..78696453hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3839161
hg1939161
hg1839161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555472
Supporting Variants
Samples
Known GenesTENM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779323
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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