A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209285



Internal ID22357389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190673312..190692350hg38UCSC Ensembl
chr3:190391101..190410139hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3819039
hg1919039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311796, nssv14311801, nssv14311795, nssv14311800, nssv14311797, nssv14311802, nssv14311794, nssv14311799, nssv14311798
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209285
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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