A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706950



Internal ID130616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59913669..59916871hg38UCSC Ensembl
chr16:59947573..59950775hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383203
hg193203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706950
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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