A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555472



Internal ID16342881
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 StatusM
Merged Variants
Supporting Variantsnssv779323
Samples
Known GenesTENM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555472
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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