A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5836922



Internal ID8814325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126314414..126317263hg38UCSC Ensembl
chr11:126184309..126187158hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663692
Supporting Variants
SamplesNA19916
Known GenesDCPS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5836922
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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