A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023444



Internal ID83347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32463889..32463889hg38UCSC Ensembl
chr9:32463887..32463887hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544469
Supporting Variants
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023444
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.719908


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