A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587141



Internal ID7058523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646063..189653138hg38UCSC Ensembl
Innerchr3:189363852..189370927hg19UCSC Ensembl
Innerchr3:190846546..190853621hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387076
hg197076
hg187076
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989738
Supporting Variants
SamplesHuRef
Known GenesTP63
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587141
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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