A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311802



Internal ID22311726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190673312..190692350hg38UCSC Ensembl
chr3:190391101..190410139hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3819039
hg1919039
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209285
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311802
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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