A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114044



Internal ID21297310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55471747..55473950hg38UCSC Ensembl
Innerchr20:54088285..54090488hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382204
hg192204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv691n145
Supporting Variantsnssv14100767
Samplessample375
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114044
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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