A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626745



Internal ID7013575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69218226..69232991hg38UCSC Ensembl
Innerchr11:69218252..69232965hg38UCSC Ensembl
Outerchr11:69218200..69233017hg38UCSC Ensembl
chr11:68985693..69000458hg19UCSC Ensembl
Innerchr11:68985719..69000432hg19UCSC Ensembl
Outerchr11:68985667..69000484hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3814766
hg1914766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14204906
SamplesNA18557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626745
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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