A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793119



Internal ID18827516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380017..34546808hg38UCSC Ensembl
Innerchr15:34672218..34839009hg19UCSC Ensembl
Innerchr15:32459510..32626301hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38166792
hg19166792
hg18166792
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892664
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793119
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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