A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216822



Internal ID22362688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69301176..69301229hg38UCSC Ensembl
chr11:69068643..69068696hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357097
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216822
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