A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564358



Internal ID18765434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102408716..102410485hg38UCSC Ensembl
Outerchr4:102408645..102410710hg38UCSC Ensembl
Innerchr4:103329873..103331642hg19UCSC Ensembl
Outerchr4:103329802..103331867hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv332e215
Supporting Variantsessv9763105
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564358
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