A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791285



Internal ID19164379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18573422hg38UCSC Ensembl
Innerchr13:19024259..19147562hg19UCSC Ensembl
Innerchr13:17922259..18045562hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38123304
hg19123304
hg18123304
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892289
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791285
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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