A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705201



Internal ID128867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98194427..98194494hg38UCSC Ensembl
chr15:98737656..98737723hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705201
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017414


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