A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586899



Internal ID6711595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534747..73555855hg38UCSC Ensembl
Innerchr14:74001451..74022559hg19UCSC Ensembl
Innerchr14:73071204..73092312hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3821109
hg1921109
hg1821109
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990289
Supporting Variants
SamplesHuRef
Known GenesACOT1, HEATR4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586899
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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