A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100921



Internal ID21291582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35950111..35958458hg38UCSC Ensembl
Innerchr21:37322409..37330756hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg388348
hg198348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114737
Supporting Variants
Samplessample77
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100921
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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