A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669748



Internal ID9935853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116173950..116177432hg38UCSC Ensembl
Outerchr11:116173793..116177585hg38UCSC Ensembl
Innerchr11:116044667..116048149hg19UCSC Ensembl
Outerchr11:116044510..116048302hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383793
hg193793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv243e199
Supporting Variantsessv5655944
SamplesHG00260
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669748
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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