A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216777



Internal ID22362659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31820138..31823441hg38UCSC Ensembl
chr16:31831459..31834762hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14374328
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216777
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