A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667215



Internal ID9933320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62367617..62385837hg38UCSC Ensembl
chr11:62135089..62153309hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3818221
hg1918221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218e199
Supporting Variantsessv5926584
SamplesNA18628
Known GenesASRGL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667215
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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