A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708698



Internal ID132364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78137768..78138447hg38UCSC Ensembl
chr16:78171665..78172344hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523097
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.042929


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