A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565296



Internal ID6689992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:32885915..32897898hg38UCSC Ensembl
Outerchr20:31473721..31485704hg19UCSC Ensembl
Outerchr20:30937382..30949365hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3811984
hg1911984
hg1811984
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996804
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565296
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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