A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1909e59



Internal ID22763129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63091139..63092637hg38UCSC Ensembl
chr18:60758372..60759870hg19UCSC Ensembl
chr18:58909352..58910850hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3430207, esv3391756, esv3349673
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1909e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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