A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625061



Internal ID6665214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:195766..233956hg38UCSC Ensembl
chr11:195766..233956hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3838191
hg1938191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13987615, essv13987616, essv13987617
SamplesHG02836, HG01440, HG01794
Known GenesBET1L, MIR6743, ODF3, RIC8A, SIRT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625061
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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