A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014736



Internal ID22076367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10589032..10605368hg38UCSC Ensembl
Outerchr21:10585552..10606113hg38UCSC Ensembl
Innerchr21:10907089..10923425hg19UCSC Ensembl
Outerchr21:10906344..10926905hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3820562
hg1920562
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155695
Supporting Variants
Samples
Known GenesTPTE
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014736
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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