A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv402e59



Internal ID22761622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41818665..41885263hg38UCSC Ensembl
chr10:42355001..42421544hg19UCSC Ensembl
chr10:41674952..41741550hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3866599
hg1966544
hg1866599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336598, esv3342799, esv3350084
SamplesNA19238, NA19239, NA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv402e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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