A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988039



Internal ID7060339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192672008..192674145hg38UCSC Ensembl
Innerchr3:192389797..192391934hg19UCSC Ensembl
Innerchr3:193872491..193874628hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382138
hg192138
hg182138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115e180
Supporting Variantsessv3586803
SamplesHuRef
Known GenesFGF12
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988039
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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