A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627959



Internal ID7014784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123642765..123643420hg38UCSC Ensembl
Innerchr11:123642778..123643407hg38UCSC Ensembl
Outerchr11:123642752..123643433hg38UCSC Ensembl
chr11:123513473..123514128hg19UCSC Ensembl
Innerchr11:123513486..123514115hg19UCSC Ensembl
Outerchr11:123513460..123514141hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301217
SamplesHG04194
Known GenesSCN3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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