A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv356e59



Internal ID20127105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5368989..5371487hg38UCSC Ensembl
chr10:5410952..5413450hg19UCSC Ensembl
chr10:5400952..5403450hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382499
hg192499
hg182499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3387601, esv3362564
SamplesNA19239, NA19240
Known GenesUCN3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv356e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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