A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv291n145



Internal ID22813307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46513961..46519980hg38UCSC Ensembl
chr13:47088096..47094115hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg386020
hg196020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116540, nsv3112499
Samplessample182, sample118
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv291n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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