A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2026e59



Internal ID22763246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54233964..54242586hg38UCSC Ensembl
chr19:54737840..54746438hg19UCSC Ensembl
chr19:59429652..59438250hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg388623
hg198599
hg188599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3445179, esv3402186, esv3387039
SamplesNA12891, NA12878, NA12892
Known GenesLILRA6
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2026e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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