A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2055e59



Internal ID22763275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8596371..8597769hg38UCSC Ensembl
chr2:8736501..8737899hg19UCSC Ensembl
chr2:8653952..8655350hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3429367, esv3348284
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2055e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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