A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222507



Internal ID22366566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26340085..26348365hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298448, nssv14298447
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222507
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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