A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023860



Internal ID83615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86127871..86130089hg38UCSC Ensembl
chr9:88742786..88745004hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382219
hg192219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023860
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