A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023702



Internal ID83512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36222902..36226511hg38UCSC Ensembl
chr9:36222899..36226508hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383610
hg193610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476585
Supporting Variants
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023702
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