A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100679



Internal ID21280694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40628951..40632391hg38UCSC Ensembl
Innerchr20:39257591..39261031hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383441
hg193441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110959
Supporting Variants
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100679
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