A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv520e59



Internal ID22761740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125824764..125825193hg38UCSC Ensembl
chr10:127513333..127513762hg19UCSC Ensembl
chr10:127503323..127503752hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38430
hg19430
hg18430
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302504, esv3302844
SamplesNA18502, NA12717, NA18947, NA18508, NA10851, NA18561, NA18507, NA18545, NA18870, NA07357, NA07346, NA18944, NA18558, NA18547, NA18942, NA07347, NA18571, NA12287, NA18949, NA12044, NA19239, NA12828, NA11993, NA11831, NA10847, NA12489, NA12003, NA12878, NA18579, NA18572, NA18907, NA18537, NA18566, NA19114, NA18499, NA18856, NA12892, NA18532, NA18853, NA19099, NA18555, NA18523, NA18858, NA18593, NA18576, NA12043, NA18542, NA12716, NA11881, NA18952, NA18517, NA07037, NA12763, NA18505, NA12006, NA18562
Known GenesBCCIP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv520e59
Frequency
Sample Size185
Observed Gain56
Observed Loss0
Observed Complex0
Frequencyn/a


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