A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586985



Internal ID7058367
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999356
Supporting Variants
SamplesHuRef
Known GenesSFXN2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586985
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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