A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559688



Internal ID18760764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64500967..64501027hg38UCSC Ensembl
chr11:64268439..64268499hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv66e215
Supporting Variantsessv9758435
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559688
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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