A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189791



Internal ID529135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65436468..65443599hg38UCSC Ensembl
Innerchr11:65436480..65443587hg38UCSC Ensembl
Outerchr11:65436456..65443611hg38UCSC Ensembl
chr11:65203939..65211070hg19UCSC Ensembl
Innerchr11:65203951..65211058hg19UCSC Ensembl
Outerchr11:65203927..65211082hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387132
hg197132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626674
Supporting Variants
SamplesHG00231
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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