A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009936



Internal ID7059630
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107e180
Supporting Variantsessv3587282
SamplesHuRef
Known GenesSFMBT1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009936
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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