A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527619



Internal ID303712
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 StatusM
Merged Variants
Supporting Variantsnssv17705194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527619
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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