A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv836n145



Internal ID22813852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189646772..189653182hg38UCSC Ensembl
chr3:189364561..189370971hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386411
hg196411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117257, nsv3112241, nsv3114208, nsv3113862
Samplessample425, sample133, sample313, sample83, sample144, sample413, sample359, sample282, sample406, sample93, sample50, sample365, sample146, sample135, sample125, sample421, sample165, sample88, sample28, sample394, sample310, sample307, sample392, sample270, sample160, sample153, sample56, sample362, sample49, sample79, sample418, sample137, sample302, sample43, sample253, sample177, sample243, sample77, sample1, sample318, sample23, sample174, sample275, sample236, sample324, sample286, sample86, sample163, sample411
Known GenesTP63
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv836n145
Frequency
Sample Size467
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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