A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1014n145



Internal ID22814030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18259972..18267645hg38UCSC Ensembl
chr6:18260203..18267876hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387674
hg197674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114397, nsv3110748
Samplessample72, sample138
Known GenesDEK
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1014n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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