A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115721



Internal ID21298987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:123452278..123457459hg38UCSC Ensembl
Innerchr11:123322986..123328167hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385182
hg195182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091931
Samplessample242
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115721
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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