A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701033



Internal ID124699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73690969..73690969hg38UCSC Ensembl
chr15:73983310..73983310hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421571
Supporting Variants
Samples
Known GenesCD276
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.316174


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