A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997936



Internal ID7064157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75425214..75587655hg38UCSC Ensembl
Innerchr3:75474365..75636806hg19UCSC Ensembl
Innerchr3:75557055..75719496hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38162442
hg19162442
hg18162442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586261
SamplesHuRef
Known GenesFAM86DP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997936
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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