A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564890



Internal ID7035990
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007993
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564890
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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