A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv409n145



Internal ID22813425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60590634..60594248hg38UCSC Ensembl
chr15:60882833..60886447hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383615
hg193615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111436, nsv3111100
Samplessample214, sample33
Known GenesRORA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv409n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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