A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997211



Internal ID7081181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33698938..33699901hg38UCSC Ensembl
Outerchr20:32286744..32287707hg19UCSC Ensembl
Outerchr20:31750405..31751368hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565483
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997211
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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