A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891367



Internal ID18839077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18969450..18999580hg38UCSC Ensembl
Outerchr8:18969450..19003973hg38UCSC Ensembl
Innerchr8:18826960..18857090hg19UCSC Ensembl
Outerchr8:18826960..18861483hg19UCSC Ensembl
Innerchr8:18871240..18901370hg18UCSC Ensembl
Outerchr8:18871240..18905763hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834524
hg1934524
hg1834524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789608, essv25789300, essv25789071
Samples
Known GenesPSD3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891367
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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