A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv389n145



Internal ID22813405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26502719..26507199hg38UCSC Ensembl
chr15:26747866..26752346hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116469, nsv3110381
Samplessample179, sample363
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv389n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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