A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110617



Internal ID21293883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33374309..33375384hg38UCSC Ensembl
Innerchr19:33865215..33866290hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv565n145
Supporting Variantsnssv14100538, nssv14100551
Samplessample224, sample229
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110617
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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