A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792618



Internal ID18820332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34515668hg38UCSC Ensembl
Innerchr15:34718594..34807869hg19UCSC Ensembl
Innerchr15:32505886..32595161hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3889276
hg1989276
hg1889276
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892663
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792618
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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