A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195552



Internal ID22345712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96662911..96666400hg38UCSC Ensembl
chr3:96381755..96385244hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg383490
hg193490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308891, nssv14308898, nssv14308893, nssv14308894, nssv14308897, nssv14308890, nssv14308895, nssv14308892, nssv14308896
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)nsv3195552
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer