A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709771



Internal ID133437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80806706..80852982hg38UCSC Ensembl
chr16:80840603..80886879hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3846277
hg1946277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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