A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv717e59



Internal ID22761937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126449547..126451845hg38UCSC Ensembl
chr11:126319442..126321740hg19UCSC Ensembl
chr11:125824652..125826950hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3363799, esv3380656, esv3397647
SamplesNA19238, NA19239, NA19240
Known GenesKIRREL3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv717e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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