A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226579



Internal ID22369331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20421494..22369633hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381948140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258238
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226579
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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