A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701114



Internal ID124780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41303552..41328055hg38UCSC Ensembl
chr15:41595750..41620253hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3824504
hg1924504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500210
Supporting Variants
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701114
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