A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627745



Internal ID7014573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111875728..111886589hg38UCSC Ensembl
chr11:111746452..111757313hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3810862
hg1910862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14287037
SamplesHG02757
Known GenesC11orf1, FDXACB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627745
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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