A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv322n145



Internal ID22813338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29698063..29701891hg38UCSC Ensembl
chr14:30167269..30171097hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383829
hg193829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110438, nsv3113740
Samplessample143, sample411
Known GenesMIR548AI, PRKD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv322n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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