A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710076



Internal ID133742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64041461..64081871hg38UCSC Ensembl
chr16:64075365..64115775hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840411
hg1940411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004372


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