A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025615



Internal ID84811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87713485..87722384hg38UCSC Ensembl
chr9:90328400..90337299hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025615
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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