A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2432e59



Internal ID22763652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43325798..43326296hg38UCSC Ensembl
chr20:41954438..41954936hg19UCSC Ensembl
chr20:41387852..41388350hg18UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3427469, esv3384372, esv3427358
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2432e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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