A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14291877



Internal ID3476489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797581..116802941hg38UCSC Ensembl
Innerchr11:116797902..116802881hg38UCSC Ensembl
Outerchr11:116797417..116803105hg38UCSC Ensembl
chr11:116668297..116673657hg19UCSC Ensembl
Innerchr11:116668618..116673597hg19UCSC Ensembl
Outerchr11:116668133..116673821hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385361
hg195361
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627830
Supporting Variants
SamplesHG03091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14291877
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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