A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564357



Internal ID18765433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102408629..102410596hg38UCSC Ensembl
Outerchr4:102408254..102411135hg38UCSC Ensembl
Innerchr4:103329786..103331753hg19UCSC Ensembl
Outerchr4:103329411..103332292hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382882
hg192882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv332e215
Supporting Variantsessv9763104
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564357
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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