A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005660



Internal ID6717780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40278831..40284928hg38UCSC Ensembl
Outerchr19:40784738..40790835hg19UCSC Ensembl
Outerchr19:45476578..45482675hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386098
hg196098
hg186098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565085
SamplesHuRef
Known GenesAKT2, MIR641
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005660
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