A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704438



Internal ID128104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80261113..80261164hg38UCSC Ensembl
chr15:80553455..80553506hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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