A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv279n145



Internal ID22813295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29371809..29390700hg38UCSC Ensembl
chr13:29945946..29964837hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3818892
hg1918892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117040, nsv3113344
Samplessample68, sample110
Known GenesMTUS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv279n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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