A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003677



Internal ID7068782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87515929..87516980hg38UCSC Ensembl
Innerchr10:89275686..89276737hg19UCSC Ensembl
Innerchr10:89265666..89266717hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381052
hg191052
hg181052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586846
SamplesHuRef
Known GenesMINPP1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003677
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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