A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216920



Internal ID22362758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62403019..62421180hg38UCSC Ensembl
Outerchr15:62695218..62713379hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818162
hg1918162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258438, nssv14258441, nssv14258440, nssv14258439, nssv14258442
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216920
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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