A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997484



Internal ID7063823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61468158..61474769hg38UCSC Ensembl
Innerchr8:62380717..62387328hg19UCSC Ensembl
Innerchr8:62543271..62549882hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386612
hg196612
hg186612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv184e180
Supporting Variantsessv3586773
SamplesHuRef
Known GenesCLVS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997484
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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