A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1013n145



Internal ID22814029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15469209..15473955hg38UCSC Ensembl
chr6:15469440..15474186hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384747
hg194747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115326, nsv3110314
Samplessample417, sample385, sample331
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1013n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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