A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv407n145



Internal ID22813423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57583974..57612826hg38UCSC Ensembl
chr15:57876172..57905024hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828853
hg1928853
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114739, nsv3114710
Samplessample190, sample129
Known GenesGCOM1, MYZAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv407n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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