A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514206



Internal ID290706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100926773..100932097hg38UCSC Ensembl
chr15:101466978..101472302hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385325
hg195325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703381
Samples
Known GenesLRRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514206
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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