A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550644



Internal ID18751720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69263555..69263596hg38UCSC Ensembl
Outerchr13:69263548..69263602hg38UCSC Ensembl
Innerchr13:69837687..69837728hg19UCSC Ensembl
Outerchr13:69837680..69837734hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749391
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550644
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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