A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660519



Internal ID9926624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103386704..103815015hg38UCSC Ensembl
chr11:103257432..103685743hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38428312
hg19428312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5808160
SamplesHG00732
Known GenesDYNC2H1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660519
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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