A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14288020



Internal ID2241486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113531833..113533122hg38UCSC Ensembl
Innerchr11:113531850..113533106hg38UCSC Ensembl
Outerchr11:113531817..113533139hg38UCSC Ensembl
chr11:113402555..113403844hg19UCSC Ensembl
Innerchr11:113402572..113403828hg19UCSC Ensembl
Outerchr11:113402539..113403861hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627778
Supporting Variants
SamplesHG02010
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14288020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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