A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547895



Internal ID18748971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63931768..63934158hg38UCSC Ensembl
Outerchr11:63931322..63934210hg38UCSC Ensembl
Innerchr11:63699240..63701630hg19UCSC Ensembl
Outerchr11:63698794..63701682hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746642
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547895
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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