A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099202



Internal ID21272762
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 StatusS
Merged Variantsnsv3116051
Supporting Variants
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099202
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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