A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1411e59



Internal ID22762631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026562..45032160hg38UCSC Ensembl
chr15:45318760..45324358hg19UCSC Ensembl
chr15:43106052..43111650hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385599
hg195599
hg185599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3401551, esv3370250
SamplesNA19239, NA19240
Known GenesSORD
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1411e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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