A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562889



Internal ID18763965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169020689..169021007hg38UCSC Ensembl
Outerchr3:169020614..169021092hg38UCSC Ensembl
Innerchr3:168738477..168738795hg19UCSC Ensembl
Outerchr3:168738402..168738880hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761636
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562889
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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