A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797262



Internal ID18816645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80633514..80650401hg38UCSC Ensembl
Innerchr7:80262830..80279717hg19UCSC Ensembl
Innerchr7:80100766..80117653hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3816888
hg1916888
hg1816888
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=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797262
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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