A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29976



Internal ID12608170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10345209..10646524hg38UCSC Ensembl
Innerchr21:10865933..11167248hg19UCSC Ensembl
Innerchr21:9887804..10189119hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38301316
hg19301316
hg18301316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84215
SamplesHuRef
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29976
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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