A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220510



Internal ID22365184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43961575..43961681hg38UCSC Ensembl
chr21:45381456..45381562hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300975, nssv14300973, nssv14300974, nssv14300972
SamplesNA19238, NA19239, NA19240, HG00513
Known GenesAGPAT3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220510
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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