A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789741



Internal ID19182006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18510660hg38UCSC Ensembl
Innerchr13:19024259..19084800hg19UCSC Ensembl
Innerchr13:17922259..17982800hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3860542
hg1960542
hg1860542
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892288
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789741
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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