A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216220



Internal ID22362286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4199026..4218869hg38UCSC Ensembl
Outerchr16:4249027..4268870hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819844
hg1919844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3122n152
Supporting Variantsnssv14260212
SamplesNA19240
Known GenesSRL
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216220
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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