A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586780



Internal ID7058162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103895643..103896831hg38UCSC Ensembl
Innerchr14:104361980..104363168hg19UCSC Ensembl
Innerchr14:103431733..103432921hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381189
hg191189
hg181189
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997353
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586780
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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