A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110872



Internal ID21294138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47151692..47162057hg38UCSC Ensembl
Innerchr20:45780331..45790696hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810366
hg1910366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv689n145
Supporting Variantsnssv14099935
Samplessample210
Known GenesEYA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110872
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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