A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066089



Internal ID21975322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93704307..93704307hg38UCSC Ensembl
chr8:94716535..94716535hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591978
Samples
Known GenesFAM92A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066089
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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