A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705796



Internal ID129462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23454618..23455552hg38UCSC Ensembl
chr16:23465939..23466873hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006565


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