A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702226



Internal ID125892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84916173..84916240hg38UCSC Ensembl
chr15:85459404..85459471hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534678
Supporting Variants
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702226
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.262269


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