A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892678



Internal ID18836812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42130892..42138944hg38UCSC Ensembl
Outerchr15:42130892..42142055hg38UCSC Ensembl
Innerchr15:42423090..42431142hg19UCSC Ensembl
Outerchr15:42423090..42434253hg19UCSC Ensembl
Innerchr15:40210382..40218434hg18UCSC Ensembl
Outerchr15:40210382..40221545hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3811164
hg1911164
hg1811164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780063, essv25796312, essv25798316, essv25798470, essv25797675, essv25796308, essv25780444, essv25781615, essv25786664, essv25785465
Samples
Known GenesPLA2G4F
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892678
Frequency
Sample Size3017
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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