A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547694



Internal ID18748770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45822807..45823847hg38UCSC Ensembl
Outerchr11:45822643..45823891hg38UCSC Ensembl
Innerchr11:45844358..45845398hg19UCSC Ensembl
Outerchr11:45844194..45845442hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746441
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547694
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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