A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv728e59



Internal ID22761948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133932447..133933145hg38UCSC Ensembl
chr11:133802342..133803040hg19UCSC Ensembl
chr11:133307552..133308250hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3381122, esv3366951
SamplesNA19238, NA19240
Known GenesIGSF9B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv728e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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