A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214927



Internal ID22361427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84226006..84432121hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38206116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3010n152
Supporting Variantsnssv14258834, nssv14258830, nssv14258837, nssv14258835, nssv14258832, nssv14258833, nssv14258831, nssv14258836
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214927
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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