A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565776



Internal ID7037158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:5031094..5037157hg38UCSC Ensembl
Outerchr20:5011740..5017803hg19UCSC Ensembl
Outerchr20:4959740..4965803hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386064
hg196064
hg186064
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003384
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565776
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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