A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788141



Internal ID18836247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4499361..4515982hg38UCSC Ensembl
Innerchr9:4499361..4515982hg19UCSC Ensembl
Innerchr9:4489361..4505982hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3816622
hg1916622
hg1816622
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891532
Supporting Variants
Samples
Known GenesSLC1A1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788141
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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