A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891532



Internal ID18839242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4499361..4515982hg38UCSC Ensembl
Outerchr9:4499361..4515982hg38UCSC Ensembl
Innerchr9:4499361..4515982hg19UCSC Ensembl
Outerchr9:4499361..4515982hg19UCSC Ensembl
Innerchr9:4489361..4505982hg18UCSC Ensembl
Outerchr9:4489361..4505982hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3816622
hg1916622
hg1816622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788141
Samples
Known GenesSLC1A1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891532
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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