A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2857791



Internal ID10877488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70371324..70371560hg38UCSC Ensembl
Outerchr11:70217430..70217666hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7127358
SamplesHuRef
Known GenesPPFIA1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2857791
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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