A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093356



Internal ID22002589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92098967..92098967hg38UCSC Ensembl
chr14:92565311..92565311hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610221
Samples
Known GenesATXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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