A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705194



Internal ID128860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98086312..98100229hg38UCSC Ensembl
chr15:98629541..98643458hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3813918
hg1913918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705194
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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