A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115029



Internal ID21298295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86379175..86386104hg38UCSC Ensembl
Innerchr16:86412781..86419710hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386930
hg196930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097892
Samplessample397
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115029
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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