A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008480



Internal ID7073457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114611550..114626400hg38UCSC Ensembl
Outerchr9:117373830..117388680hg19UCSC Ensembl
Outerchr9:116413651..116428501hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814851
hg1914851
hg1814851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564147
SamplesHuRef
Known GenesC9orf91
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008480
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