A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015868



Internal ID78226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106027657..106039033hg38UCSC Ensembl
chr8:107039885..107051261hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3811377
hg1911377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015868
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