A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2899e59



Internal ID22764119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197032884..197035382hg38UCSC Ensembl
chr3:196759755..196762253hg19UCSC Ensembl
chr3:198244152..198246650hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382499
hg192499
hg182499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3353278, esv3335242, esv3347297
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2899e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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