A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17008242



Internal ID73123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8721235..8773611hg38UCSC Ensembl
chr8:8578745..8631121hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3852377
hg1952377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17008242
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer