A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892291



Internal ID19183111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18648432..18803539hg38UCSC Ensembl
Outerchr13:18573422..18803539hg38UCSC Ensembl
Innerchr13:19222572..19377679hg19UCSC Ensembl
Outerchr13:19147562..19377679hg19UCSC Ensembl
Innerchr13:18120572..18275679hg18UCSC Ensembl
Outerchr13:18045562..18275679hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38230118
hg19230118
hg18230118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790629, essv25792817, essv25792461, essv25791517
Samples
Known GenesLINC00417
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892291
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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