A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016804



Internal ID78859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111555055..111710524hg38UCSC Ensembl
chr8:112567284..112722753hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38155470
hg19155470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016804
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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