A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788954



Internal ID19159782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69238120..69355049hg38UCSC Ensembl
Innerchr13:69812252..69929181hg19UCSC Ensembl
Innerchr13:68710253..68827182hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38116930
hg19116930
hg18116930
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892385
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788954
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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