A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1711e59



Internal ID22762931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20467447..20470645hg38UCSC Ensembl
chr17:20370760..20373958hg19UCSC Ensembl
chr17:20311352..20314550hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383199
hg193199
hg183199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3398249, esv3418727
SamplesNA19239, NA19240
Known GenesLGALS9B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1711e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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