A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117784



Internal ID21301050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11249789..11251669hg38UCSC Ensembl
Innerchr20:11230437..11232317hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100768
Samplessample378
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117784
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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