A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627244



Internal ID7014074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91316893..91405510hg38UCSC Ensembl
Innerchr11:91316908..91405495hg38UCSC Ensembl
Outerchr11:91316878..91405525hg38UCSC Ensembl
chr11:91050060..91138676hg19UCSC Ensembl
Innerchr11:91050075..91138661hg19UCSC Ensembl
Outerchr11:91050045..91138691hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3888618
hg1988617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14233024
SamplesHG00452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627244
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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