A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006987



Internal ID7072080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:64127108..64138688hg38UCSC Ensembl
Outerchr20:62758461..62770041hg19UCSC Ensembl
Outerchr20:62228905..62240485hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811581
hg1911581
hg1811581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565235
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006987
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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