A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626927



Internal ID7013757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80044094..80124843hg38UCSC Ensembl
Innerchr11:80044133..80124804hg38UCSC Ensembl
Outerchr11:80044055..80124882hg38UCSC Ensembl
chr11:79755137..79835887hg19UCSC Ensembl
Innerchr11:79755176..79835848hg19UCSC Ensembl
Outerchr11:79755098..79835926hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3880750
hg1980751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216132
SamplesHG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626927
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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