A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535006



Internal ID22404267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9213104..9213378hg38UCSC Ensembl
chr20:9193751..9194025hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298606
SamplesNA19239
Known GenesPLCB4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535006
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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