A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587282



Internal ID7058664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52993109..53004960hg38UCSC Ensembl
Innerchr3:53027125..53038976hg19UCSC Ensembl
Innerchr3:53002165..53014016hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3811852
hg1911852
hg1811852
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009936
Supporting Variants
SamplesHuRef
Known GenesSFMBT1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587282
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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