A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222734



Internal ID22366714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:25602541..25632343hg38UCSC Ensembl
Outerchr16:25613862..25643664hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3829803
hg1929803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259697
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222734
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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