A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29983



Internal ID12954863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149433515..149484515hg38UCSC Ensembl
Innerchr3:149151302..149202302hg19UCSC Ensembl
Innerchr3:150633992..150684992hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3851001
hg1951001
hg1851001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84222
SamplesHuRef
Known GenesTM4SF4
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29983
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer