A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710231



Internal ID133897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84697570..84697993hg38UCSC Ensembl
chr16:84731176..84731599hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710231
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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