A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990845



Internal ID7076976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:813931..823612hg38UCSC Ensembl
Outerchr17:717171..726852hg19UCSC Ensembl
Outerchr17:663921..673602hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg389682
hg199682
hg189682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565225
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990845
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