A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv528e59



Internal ID22761748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133121058..133122156hg38UCSC Ensembl
chr10:134934562..134935660hg19UCSC Ensembl
chr10:134784552..134785650hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3417465, esv3363946
SamplesNA19239, NA19240
Known GenesGPR123
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv528e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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