A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526414



Internal ID302545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99198066..99388066hg38UCSC Ensembl
chr15:99738271..99928271hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38190001
hg19190001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705275
Samples
Known GenesHSP90B2P, LRRC28, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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