A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2796e59



Internal ID22764016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129369319..129371217hg38UCSC Ensembl
chr3:129088162..129090060hg19UCSC Ensembl
chr3:130570852..130572750hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3388276, esv3332438, esv3413638
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2796e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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