A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2081e59



Internal ID18987582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25399657..25399838hg38UCSC Ensembl
chr2:25622526..25622707hg19UCSC Ensembl
chr2:25476030..25476211hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38182
hg19182
hg18182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3414045, esv3364916
SamplesNA19240
Known GenesDTNB
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2081e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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