A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14216042



Internal ID5803728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79679407..79684846hg38UCSC Ensembl
Innerchr11:79679510..79684708hg38UCSC Ensembl
Outerchr11:79679153..79685100hg38UCSC Ensembl
chr11:79390451..79395890hg19UCSC Ensembl
Innerchr11:79390554..79395752hg19UCSC Ensembl
Outerchr11:79390197..79396144hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385440
hg195440
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626921
Supporting Variants
SamplesNA19175
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14216042
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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