A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796312



Internal ID18826595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42130892..42142055hg38UCSC Ensembl
Innerchr15:42423090..42434253hg19UCSC Ensembl
Innerchr15:40210382..40221545hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3811164
hg1911164
hg1811164
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892678
Supporting Variants
Samples
Known GenesPLA2G4F
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796312
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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