A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999860



Internal ID7082468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:8057040..8066417hg38UCSC Ensembl
Outerchr16:8107042..8116419hg19UCSC Ensembl
Outerchr16:8047043..8056420hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg389378
hg199378
hg189378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565555
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999860
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer