A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2622e59



Internal ID22763842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44333415..44336406hg38UCSC Ensembl
chr22:44729295..44732286hg19UCSC Ensembl
chr22:43107952..43110950hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382992
hg192992
hg182999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3392869, esv3414874, esv3412325, esv3362936, esv3437435
SamplesNA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2622e59
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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