A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215156



Internal ID22361582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:11340358..11357279hg38UCSC Ensembl
Outerchr20:11321006..11337927hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3816922
hg1916922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266623
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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