A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005893



Internal ID7070987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:33403833..33410758hg38UCSC Ensembl
Outerchr13:33977970..33984895hg19UCSC Ensembl
Outerchr13:32875970..32882895hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg386926
hg196926
hg186926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565249
SamplesHuRef
Known GenesSTARD13
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005893
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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