A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562047



Internal ID18763123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:70612351..70612516hg38UCSC Ensembl
Outerchr3:70612349..70612535hg38UCSC Ensembl
Innerchr3:70661502..70661667hg19UCSC Ensembl
Outerchr3:70661500..70661686hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760794
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562047
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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