A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003258



Internal ID7068367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:43356230..43366717hg38UCSC Ensembl
Outerchr20:41984870..41995357hg19UCSC Ensembl
Outerchr20:41418284..41428771hg18UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg3810488
hg1910488
hg1810488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565782
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003258
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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