A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211525



Internal ID22359057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:29690720..29723613hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3832894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5223n152
Supporting Variantsnssv14266662, nssv14266661
SamplesNA19238, HG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211525
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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