A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246368



Internal ID22376389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89730757..89739701hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253206
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246368
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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