A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110760



Internal ID21294026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13952338..13957918hg38UCSC Ensembl
Innerchr19:14063150..14068730hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385581
hg195581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101327
Samplessample295
Known GenesDCAF15, PODNL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110760
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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