A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996460



Internal ID7080655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67517388..67518024hg38UCSC Ensembl
Innerchr14:67984105..67984741hg19UCSC Ensembl
Innerchr14:67053858..67054494hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38637
hg19637
hg18637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586535
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996460
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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