A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710279



Internal ID133945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85450225..85450557hg38UCSC Ensembl
chr16:85483831..85484163hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710279
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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