A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562883



Internal ID18763959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167395465..167399077hg38UCSC Ensembl
Outerchr3:167395432..167399087hg38UCSC Ensembl
Innerchr3:167113253..167116865hg19UCSC Ensembl
Outerchr3:167113220..167116875hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg383656
hg193656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761630
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562883
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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