A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023663



Internal ID83487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35603996..35604014hg38UCSC Ensembl
chr9:35603993..35604011hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023663
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006402


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