A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707149



Internal ID130815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69853069..69861084hg38UCSC Ensembl
chr16:69886972..69894987hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388016
hg198016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519250
Supporting Variants
Samples
Known GenesWWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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