A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111332



Internal ID21294598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33901160..33904455hg38UCSC Ensembl
Innerchr19:34392065..34395360hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100484
Samplessample206
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111332
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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