A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025428



Internal ID84686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060413..87068100hg38UCSC Ensembl
chr9:89675328..89683015hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387688
hg197688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002498


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