A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999288



Internal ID7082123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:98591255..98604780hg38UCSC Ensembl
Outerchr5:97926959..97940484hg19UCSC Ensembl
Outerchr5:97954859..97968384hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3813526
hg1913526
hg1813526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565294
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999288
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