A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789413



Internal ID19160940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39228558..39256126hg38UCSC Ensembl
Innerchr15:39520759..39548327hg19UCSC Ensembl
Innerchr15:37308051..37335619hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3827569
hg1927569
hg1827569
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892677
Supporting Variants
Samples
Known GenesC15orf54
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789413
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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