A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093610



Internal ID22002843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87365010..87365010hg38UCSC Ensembl
chr16:87398616..87398616hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624586
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093610
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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