A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007993



Internal ID7073087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:72263269..72274091hg38UCSC Ensembl
Outerchr13:72837407..72848229hg19UCSC Ensembl
Outerchr13:71735408..71746230hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3810823
hg1910823
hg1810823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564890
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007993
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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