A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564314



Internal ID7035414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:7113326..7123244hg38UCSC Ensembl
Outerchr20:7093973..7103891hg19UCSC Ensembl
Outerchr20:7041973..7051891hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg389919
hg199919
hg189919
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006515
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564314
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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