A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565207



Internal ID18766283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186625993..186626997hg38UCSC Ensembl
Outerchr4:186625941..186627043hg38UCSC Ensembl
Innerchr4:187547147..187548151hg19UCSC Ensembl
Outerchr4:187547095..187548197hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763954
Samples
Known GenesFAT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565207
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