A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14291944



Internal ID3500100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116809983..116813169hg38UCSC Ensembl
Innerchr11:116810003..116813150hg38UCSC Ensembl
Outerchr11:116809964..116813189hg38UCSC Ensembl
chr11:116680699..116683885hg19UCSC Ensembl
Innerchr11:116680719..116683866hg19UCSC Ensembl
Outerchr11:116680680..116683905hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383187
hg193187
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627831
Supporting Variants
SamplesHG03108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14291944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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