A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215418



Internal ID22361762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33474797..33476761hg38UCSC Ensembl
chr8:33332315..33334279hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381965
hg191965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340511
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215418
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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