A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2908e59



Internal ID22764128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198227984..198235559hg38UCSC Ensembl
chr3:197954855..197962430hg19UCSC Ensembl
chr3:199439252..199446850hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387576
hg197576
hg187599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3332191, esv3428779, esv3352805, esv3411930, esv3414359, esv3450599
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2908e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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