A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028199



Internal ID86495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106546329..106546405hg38UCSC Ensembl
chr9:109308610..109308686hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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