A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv716e59



Internal ID20127465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126436747..126438245hg38UCSC Ensembl
chr11:126306642..126308140hg19UCSC Ensembl
chr11:125811852..125813350hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3380455, esv3428191
SamplesNA19239, NA19240
Known GenesKIRREL3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv716e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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