A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709458



Internal ID133124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57292242..57294248hg38UCSC Ensembl
chr16:57326154..57328160hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709458
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.317315


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