A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626807



Internal ID7013637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72908366..72914454hg38UCSC Ensembl
Innerchr11:72908390..72914430hg38UCSC Ensembl
Outerchr11:72908342..72914478hg38UCSC Ensembl
chr11:72619411..72625499hg19UCSC Ensembl
Innerchr11:72619435..72625475hg19UCSC Ensembl
Outerchr11:72619387..72625523hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386089
hg196089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14212059
SamplesNA20536
Known GenesFCHSD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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