A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550785



Internal ID18751861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83372505..83380192hg38UCSC Ensembl
Outerchr13:83372318..83381365hg38UCSC Ensembl
Innerchr13:83946640..83954327hg19UCSC Ensembl
Outerchr13:83946453..83955500hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg389048
hg199048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749532
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550785
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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