A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702340



Internal ID126006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70541046..70541149hg38UCSC Ensembl
chr15:70833385..70833488hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702340
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002032


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