A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000667



Internal ID6712809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:98892507..98895886hg38UCSC Ensembl
Innerchr4:99813658..99817037hg19UCSC Ensembl
Innerchr4:100032681..100036060hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg383380
hg193380
hg183380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586866
SamplesHuRef
Known GenesEIF4E
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000667
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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