A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586773



Internal ID7058155
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv997484
Supporting Variants
SamplesHuRef
Known GenesCLVS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586773
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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