A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1825e59



Internal ID18987326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79042575..79043973hg38UCSC Ensembl
chr17:77038657..77040055hg19UCSC Ensembl
chr17:74550252..74551650hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3444941, esv3381404, esv3397230
SamplesNA19239, NA19238, NA19240
Known GenesC1QTNF1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1825e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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