A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099998



Internal ID21277795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47151692..47161308hg38UCSC Ensembl
Innerchr20:45780331..45789947hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389617
hg199617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118064
Supporting Variants
Samplessample259
Known GenesEYA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099998
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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