A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203488



Internal ID22352490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154795452..154796561hg38UCSC Ensembl
chr3:154513241..154514350hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308373, nssv14308365, nssv14308370, nssv14308366, nssv14308371, nssv14308369, nssv14308367, nssv14308368, nssv14308372
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)nsv3203488
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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