A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096343



Internal ID21276194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69053612..69069681hg38UCSC Ensembl
Innerchr16:69087515..69103584hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816070
hg1916070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113102
Supporting Variants
Samplessample233
Known GenesTANGO6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096343
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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