A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2623e59



Internal ID22763843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45979308..45981306hg38UCSC Ensembl
chr22:46375188..46377186hg19UCSC Ensembl
chr22:44753852..44755850hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381999
hg191999
hg181999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3334016, esv3403164
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2623e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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