A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586082



Internal ID7057464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82401376..82508838hg38UCSC Ensembl
Innerchr15:82693587..82793246hg19UCSC Ensembl
Innerchr15:80480642..80580301hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38107463
hg1999660
hg1899660
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999520
Supporting Variants
SamplesHuRef
Known GenesCSPG4P8, GOLGA6L20, GOLGA6L9, LOC440300, LOC80154, UBE2Q2P2, UBE2Q2P3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586082
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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