A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556249



Internal ID18757325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband19q12
Allele length
AssemblyAllele length
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv220e215
Supporting Variantsessv9754996
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556249
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