A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626672



Internal ID7013504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65323729..65331202hg38UCSC Ensembl
Innerchr11:65323729..65331202hg38UCSC Ensembl
Outerchr11:65323522..65331412hg38UCSC Ensembl
chr11:65091200..65098673hg19UCSC Ensembl
Innerchr11:65091200..65098673hg19UCSC Ensembl
Outerchr11:65090993..65098883hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387474
hg197474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14189789
SamplesHG02772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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