A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709540



Internal ID133206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58775910..58778292hg38UCSC Ensembl
chr16:58809814..58812196hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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