A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009993



Internal ID74303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26157843..26160185hg38UCSC Ensembl
chr8:26015359..26017701hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg382343
hg192343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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