A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029424



Internal ID21938767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100982093..100982170hg38UCSC Ensembl
chr15:101522298..101522375hg19UCSC 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 Variantsnssv17613952
Samples
Known GenesLRRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029424
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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