A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097836



Internal ID22007069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99886900..99886900hg38UCSC Ensembl
chr9:102649182..102649182hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585817
Samples
Known GenesLOC441461
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097836
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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