A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009879



Internal ID74233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23267783..23268166hg38UCSC Ensembl
chr8:23125296..23125679hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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