A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626674



Internal ID7013506
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14189791
SamplesHG00231
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626674
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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