A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099271



Internal ID21275443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53850162..53852649hg38UCSC Ensembl
Innerchr16:53884074..53886561hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382488
hg192488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114559
Supporting Variants
Samplessample222
Known GenesFTO
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099271
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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