A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992691



Internal ID7062184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:103533900..103540938hg38UCSC Ensembl
Outerchr3:103252744..103259782hg19UCSC Ensembl
Outerchr3:104735434..104742472hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565099
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992691
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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