A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216953



Internal ID22362776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:30130684..30167515hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3836832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266266
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216953
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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