A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627481



Internal ID7014310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100410128..100522832hg38UCSC Ensembl
Innerchr11:100410155..100522805hg38UCSC Ensembl
Outerchr11:100410101..100522859hg38UCSC Ensembl
chr11:100280859..100393563hg19UCSC Ensembl
Innerchr11:100280886..100393536hg19UCSC Ensembl
Outerchr11:100280832..100393590hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38112705
hg19112705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv227e214
Supporting Variantsessv14250878, essv14250877, essv14250879, essv14250876
SamplesHG01860, HG01801, HG01794, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627481
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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