A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307226



Internal ID22258896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28994409..29001288hg38UCSC Ensembl
chr3:29035900..29042779hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386880
hg196880
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194779
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307226
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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