A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117746



Internal ID21301012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115360397..115369353hg38UCSC Ensembl
Innerchr11:115231116..115240071hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388957
hg198956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091843
Samplessample205
Known GenesCADM1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117746
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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