A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417697



Internal ID196888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79126715..79126766hg38UCSC Ensembl
chr15:79419057..79419108hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417697
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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