A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215326



Internal ID22361697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:19918449..19962160hg38UCSC Ensembl
Outerchr16:19929771..19973482hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3843712
hg1943712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14260298, nssv14260297
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215326
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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