A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218306



Internal ID22363691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86531383..86589582hg38UCSC Ensembl
Outerchr9:89146298..89204497hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3858200
hg1958200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282857
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218306
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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