A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543606



Internal ID18744682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66208577..66209376hg38UCSC Ensembl
Outerchr8:66208477..66209577hg38UCSC Ensembl
Innerchr8:67120812..67121611hg19UCSC Ensembl
Outerchr8:67120712..67121812hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742353
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543606
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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