A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584814



Internal ID21533358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100982051..100982128hg38UCSC Ensembl
chr15:101522256..101522333hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093129
SamplesHG03683
Known GenesLRRK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584814
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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