A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002669



Internal ID7067784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130599850..130600436hg38UCSC Ensembl
Innerchr9:133475237..133475823hg19UCSC Ensembl
Innerchr9:132465058..132465644hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38587
hg19587
hg18587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586328
SamplesHuRef
Known GenesFUBP3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002669
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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