A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113935



Internal ID21297201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115331464..115343454hg38UCSC Ensembl
Innerchr11:115202183..115214173hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811991
hg1911991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090258
Samplessample397
Known GenesCADM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113935
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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