A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243477



Internal ID4702066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95371584..95372357hg38UCSC Ensembl
Innerchr11:95371589..95372352hg38UCSC Ensembl
Outerchr11:95371579..95372362hg38UCSC Ensembl
chr11:95104748..95105521hg19UCSC Ensembl
Innerchr11:95104753..95105516hg19UCSC Ensembl
Outerchr11:95104743..95105526hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627346
Supporting Variants
SamplesHG04222
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243477
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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