A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225669



Internal ID22368731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:16065108..16087804hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5651n152
Supporting Variantsnssv14269382
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225669
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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