A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089096



Internal ID21998329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99404363..99404363hg38UCSC Ensembl
chr9:102166645..102166645hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089096
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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