A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv736n145



Internal ID22813752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40042966..40046479hg38UCSC Ensembl
chr22:40438970..40442483hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383514
hg193514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115380, nsv3116602, nsv3110623
Samplessample306, sample310, sample309
Known GenesTNRC6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv736n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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