A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628090



Internal ID7014915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130753921..130759137hg38UCSC Ensembl
Innerchr11:130753971..130759087hg38UCSC Ensembl
Outerchr11:130753871..130759187hg38UCSC Ensembl
chr11:130623816..130629032hg19UCSC Ensembl
Innerchr11:130623866..130628982hg19UCSC Ensembl
Outerchr11:130623766..130629082hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg385217
hg195217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14312661, essv14312660, essv14312658, essv14312659
SamplesNA19055, NA18988, NA18986, NA19000
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628090
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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