A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1357e59



Internal ID22762577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20455785..20464383hg38UCSC Ensembl
chr15:20661038..20669636hg19UCSC Ensembl
chr15:18921052..18929650hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg388599
hg198599
hg188599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3419194, esv3417584
SamplesNA19238, NA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1357e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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