A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv522e59



Internal ID22761742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125923393..125928391hg38UCSC Ensembl
chr10:127611962..127616960hg19UCSC Ensembl
chr10:127601952..127606950hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg384999
hg194999
hg184999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3352961, esv3425912
SamplesNA12891, NA19239
Known GenesFANK1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv522e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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