A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14278492



Internal ID3046389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109177288..109190924hg38UCSC Ensembl
chr11:109048015..109061651hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3813637
hg1913637
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627694
Supporting Variants
SamplesHG02681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14278492
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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