A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021685



Internal ID82112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17645668..17719793hg38UCSC Ensembl
chr9:17645666..17719791hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3874126
hg1974126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491606
Supporting Variants
Samples
Known GenesSH3GL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021685
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