A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555676



Internal ID18756752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75559833..75560219hg38UCSC Ensembl
Outerchr18:75559753..75560221hg38UCSC Ensembl
Innerchr18:73271788..73272174hg19UCSC Ensembl
Outerchr18:73271708..73272176hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv209e215
Supporting Variantsessv9754423
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555676
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