A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707099



Internal ID130765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62902362..62906479hg38UCSC Ensembl
chr16:62936266..62940383hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384118
hg194118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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