A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29981



Internal ID12608175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105505557..106312333hg38UCSC Ensembl
Innerchr14:105971894..106768594hg19UCSC Ensembl
Innerchr14:105042939..105839639hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38806777
hg19796701
hg18796701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84220
SamplesHuRef
Known GenesADAM6, ELK2AP, KIAA0125, LINC00226, MIR8071-1, MIR8071-2, TMEM121
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29981
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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