A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097919



Internal ID21288156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80800244..80806983hg38UCSC Ensembl
Innerchr16:80834141..80840880hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg386740
hg196740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118282
Supporting Variants
Samplessample412
Known GenesCDYL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097919
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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