A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv516e59



Internal ID22761736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122724546..122726044hg38UCSC Ensembl
chr10:124484062..124485560hg19UCSC Ensembl
chr10:124474052..124475550hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3413737, esv3359904
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv516e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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