A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2634e59



Internal ID20129383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:261769..262667hg38UCSC Ensembl
chr3:303452..304350hg19UCSC Ensembl
chr3:278452..279350hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3418826, esv3418385, esv3444075
SamplesNA12891, NA12878, NA19240
Known GenesCHL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2634e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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