A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29971



Internal ID12608165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144068526..144172197hg38UCSC Ensembl
Innerchr8:145123429..145227100hg19UCSC Ensembl
Innerchr8:145195417..145299088hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38103672
hg19103672
hg18103672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84210
SamplesHuRef
Known GenesCYC1, EXOSC4, FAM203A, GPAA1, KIAA1875, MAF1, MIR6847, MROH1, SHARPIN
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29971
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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