A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565768



Internal ID6690464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:98893686..98895795hg38UCSC Ensembl
Outerchr4:99814837..99816946hg19UCSC Ensembl
Outerchr4:100033860..100035969hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg383064
hg193064
hg183064
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997164
Supporting Variants
SamplesHuRef
Known GenesEIF4E
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565768
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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