A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011100



Internal ID75046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28622831..28622896hg38UCSC Ensembl
chr8:28480348..28480413hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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