A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116051



Internal ID21299317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12829716..12838839hg38UCSC Ensembl
Innerchr16:12923573..12932696hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg389124
hg199124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099202
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116051
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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