A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099298



Internal ID22008531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92844790..92844790hg38UCSC Ensembl
chr10:94604547..94604547hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595453
Samples
Known GenesEXOC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099298
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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