A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565878



Internal ID18766954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:45005399..45013435hg38UCSC Ensembl
Outerchr5:45004399..45014898hg38UCSC Ensembl
Innerchr5:45005501..45013537hg19UCSC Ensembl
Outerchr5:45004501..45015000hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764625
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565878
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