A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705229



Internal ID128895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98601183..98607343hg38UCSC Ensembl
chr15:99144412..99150572hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386161
hg196161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705229
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003279


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