A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586621



Internal ID7058003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:66376009..66378138hg38UCSC Ensembl
Innerchr8:67288244..67290373hg19UCSC Ensembl
Innerchr8:67450798..67452927hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382130
hg192130
hg182130
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007778
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586621
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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