A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709514



Internal ID133180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58306706..58308427hg38UCSC Ensembl
chr16:58340610..58342331hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381722
hg191722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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