A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892293



Internal ID19183113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18496077..18737640hg38UCSC Ensembl
Outerchr13:18450119..18803539hg38UCSC Ensembl
Innerchr13:19070217..19311780hg19UCSC Ensembl
Outerchr13:19024259..19377679hg19UCSC Ensembl
Innerchr13:17968217..18209780hg18UCSC Ensembl
Outerchr13:17922259..18275679hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38353421
hg19353421
hg18353421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792230, essv25790097, essv25791954, essv25792011, essv25791609, essv25791386
Samples
Known GenesLINC00417
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892293
Frequency
Sample Size3017
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer