A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995059



Internal ID7079594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11245220..11248970hg38UCSC Ensembl
Outerchr11:11266767..11270517hg19UCSC Ensembl
Outerchr11:11223343..11227093hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385110
hg195110
hg185110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565535
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995059
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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