A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550951



Internal ID18752027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98069016..98069298hg38UCSC Ensembl
Outerchr13:98068955..98069343hg38UCSC Ensembl
Innerchr13:98721270..98721552hg19UCSC Ensembl
Outerchr13:98721209..98721597hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749698
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550951
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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