A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093099



Internal ID22002332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26842786..26842786hg38UCSC Ensembl
chr15:27087933..27087933hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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