A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626901



Internal ID7013731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78476573..78486191hg38UCSC Ensembl
Innerchr11:78476635..78486130hg38UCSC Ensembl
Outerchr11:78476512..78486253hg38UCSC Ensembl
chr11:78187619..78197237hg19UCSC Ensembl
Innerchr11:78187681..78197176hg19UCSC Ensembl
Outerchr11:78187558..78197299hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389619
hg199619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14215344, essv14215345
SamplesNA20517, HG00383
Known GenesNARS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626901
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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