A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763112



Internal ID18737358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102860538..102862548hg38UCSC Ensembl
Outerchr4:102860102..102862577hg38UCSC Ensembl
Innerchr4:103781695..103783705hg19UCSC Ensembl
Outerchr4:103781259..103783734hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564365
Supporting Variants
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763112
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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