A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008959



Internal ID7059005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:10763050..10772062hg38UCSC Ensembl
Outerchr5:10763162..10772174hg19UCSC Ensembl
Outerchr5:10816162..10825174hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg389013
hg199013
hg189013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565429
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008959
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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