A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891151



Internal ID18838861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80633514..80648316hg38UCSC Ensembl
Outerchr7:80633514..80656533hg38UCSC Ensembl
Innerchr7:80262830..80277632hg19UCSC Ensembl
Outerchr7:80262830..80285849hg19UCSC Ensembl
Innerchr7:80100766..80115568hg18UCSC Ensembl
Outerchr7:80100766..80123785hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3823020
hg1923020
hg1823020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796818, essv25797250, essv25798085, essv25796228, essv25796316, essv25797459, essv25796552, essv25797905, essv25797786, essv25796444, essv25797270, essv25797852, essv25796170, essv25797400, essv25796067, essv25796863, essv25797262, essv25797276, essv25796390, essv25797506, essv25797705, essv25797658, essv25796608, essv25796520, essv25796523
Samples
Known GenesCD36
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891151
Frequency
Sample Size3017
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer