A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3540898



Internal ID22410022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15216060..15219132hg38UCSC Ensembl
chr21:16588380..16591452hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383073
hg193073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300879, nssv14300881, nssv14300878, nssv14300880
SamplesHG00512, HG00732, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3540898
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