A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14265859



Internal ID22258047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:18871121..18871885hg38UCSC Ensembl
Outerchr20:18851765..18852529hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3248620
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14265859
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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