A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797276



Internal ID18835329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80633514..80656533hg38UCSC Ensembl
Innerchr7:80262830..80285849hg19UCSC Ensembl
Innerchr7:80100766..80123785hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3823020
hg1923020
hg1823020
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891151
Supporting Variants
Samples
Known GenesCD36
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797276
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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