A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791954



Internal ID19159794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18502819..18737640hg38UCSC Ensembl
Innerchr13:19076959..19311780hg19UCSC Ensembl
Innerchr13:17974959..18209780hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38234822
hg19234822
hg18234822
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892293
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791954
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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