A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225911



Internal ID22368902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3631387..3660972hg38UCSC Ensembl
Outerchr5:3631501..3661086hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7163n152
Supporting Variantsnssv14275140
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225911
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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