A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220068



Internal ID22364884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86531383..86545232hg38UCSC Ensembl
Outerchr9:89146298..89160147hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3813850
hg1913850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9634n152
Supporting Variantsnssv14282808
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220068
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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