A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993653



Internal ID7062565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10275326..10286203hg38UCSC Ensembl
Outerchr18:10275323..10286200hg19UCSC Ensembl
Outerchr18:10265323..10276200hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810878
hg1910878
hg1810878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563993
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993653
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