A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626618



Internal ID7013450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63028994..63035872hg38UCSC Ensembl
Innerchr11:63028994..63035872hg38UCSC Ensembl
Outerchr11:63028494..63036372hg38UCSC Ensembl
chr11:62796466..62803344hg19UCSC Ensembl
Innerchr11:62796466..62803344hg19UCSC Ensembl
Outerchr11:62795966..62803844hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg386879
hg196879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14182100
SamplesNA21087
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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