A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627821



Internal ID7014646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116173664..116177381hg38UCSC Ensembl
Innerchr11:116173664..116177381hg38UCSC Ensembl
Outerchr11:116173431..116177680hg38UCSC Ensembl
chr11:116044381..116048098hg19UCSC Ensembl
Innerchr11:116044381..116048098hg19UCSC Ensembl
Outerchr11:116044148..116048397hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383718
hg193718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14291029
SamplesHG00260
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627821
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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