A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3543903



Internal ID18744979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97583185..97583500hg38UCSC Ensembl
Outerchr8:97583116..97583544hg38UCSC Ensembl
Innerchr8:98595413..98595728hg19UCSC Ensembl
Outerchr8:98595344..98595772hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9742650
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3543903
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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