A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023549



Internal ID83418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33588000..33598000hg38UCSC Ensembl
chr9:33587998..33597998hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023549
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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