A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083303



Internal ID21992536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92829521..92829521hg38UCSC Ensembl
chr15:93372751..93372751hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083303
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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