A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667808



Internal ID9933913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8422993..8425058hg38UCSC Ensembl
chr11:8444540..8446605hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5523011, essv5799277, essv6405880
SamplesHG00249, HG00734, HG01125
Known GenesSTK33
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667808
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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