A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564363



Internal ID18765439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102857793..102859747hg38UCSC Ensembl
Outerchr4:102857680..102859965hg38UCSC Ensembl
Innerchr4:103778950..103780904hg19UCSC Ensembl
Outerchr4:103778837..103781122hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763110
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564363
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer