A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213584



Internal ID22360487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9907768..9912969hg38UCSC Ensembl
chr21:10385805..10390997hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg385202
hg195193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299310, nssv14299304, nssv14299308, nssv14299309, nssv14299312, nssv14299311, nssv14299306, nssv14299305, nssv14299307
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213584
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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