A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892289



Internal ID19183109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18537377hg38UCSC Ensembl
Outerchr13:18450119..18612778hg38UCSC Ensembl
Innerchr13:19024259..19111517hg19UCSC Ensembl
Outerchr13:19024259..19186918hg19UCSC Ensembl
Innerchr13:17922259..18009517hg18UCSC Ensembl
Outerchr13:17922259..18084918hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38162660
hg19162660
hg18162660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790099, essv25792286, essv25792142, essv25792356, essv25791285
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892289
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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