A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099676



Internal ID22008909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76836358..76836358hg38UCSC Ensembl
chr9:79451274..79451274hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596843
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099676
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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