A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14236538



Internal ID6807159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93286993..93296746hg38UCSC Ensembl
Innerchr11:93286994..93296745hg38UCSC Ensembl
Outerchr11:93286992..93296747hg38UCSC Ensembl
chr11:93020159..93029912hg19UCSC Ensembl
Innerchr11:93020160..93029911hg19UCSC Ensembl
Outerchr11:93020158..93029913hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389754
hg199754
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627288
Supporting Variants
SamplesNA20892
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14236538
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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