A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2610e59



Internal ID20129359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33565593..33565711hg38UCSC Ensembl
chr22:33961579..33961697hg19UCSC Ensembl
chr22:32291579..32291697hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38119
hg19119
hg18119
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302441, esv3303039
SamplesNA18861, NA18951, NA18542, NA18965, NA12044, NA12004, NA18956, NA18547, NA11995, NA18916, NA12006, NA12892, NA19238, NA19005, NA12891, NA10851, NA19138, NA12749, NA12156, NA12878, NA11993
Known GenesLARGE
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2610e59
Frequency
Sample Size185
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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