A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229884



Internal ID22371585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62952786..64321903hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381369118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282853
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229884
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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