A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893160



Internal ID18837294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5832198..5839735hg38UCSC Ensembl
Outerchr19:5827086..5839735hg38UCSC Ensembl
Innerchr19:5832209..5839746hg19UCSC Ensembl
Outerchr19:5827097..5839746hg19UCSC Ensembl
Innerchr19:5783209..5790746hg18UCSC Ensembl
Outerchr19:5778097..5790746hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812650
hg1912650
hg1812650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785153, essv25784695, essv25779959
Samples
Known GenesFUT6, NRTN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893160
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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