A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989063



Internal ID7075877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:95206175..95212609hg38UCSC Ensembl
Outerchr11:94939339..94945773hg19UCSC Ensembl
Outerchr11:94578987..94585421hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386435
hg196435
hg186435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563938
SamplesHuRef
Known GenesSESN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989063
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