A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999356



Internal ID7064875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102735122..102735790hg38UCSC Ensembl
Innerchr10:104494879..104495547hg19UCSC Ensembl
Innerchr10:104484869..104485537hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38669
hg19669
hg18669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586985
SamplesHuRef
Known GenesSFXN2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999356
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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