A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1942e59



Internal ID22763162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78605764..78607162hg38UCSC Ensembl
chr18:76365764..76367162hg19UCSC Ensembl
chr18:74466752..74468150hg18UCSC Ensembl
Cytoband18q23
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 Variantsesv3417898, esv3377950, esv3435691
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1942e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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