A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797506



Internal ID18815767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80633514..80648316hg38UCSC Ensembl
Innerchr7:80262830..80277632hg19UCSC Ensembl
Innerchr7:80100766..80115568hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3814803
hg1914803
hg1814803
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)essv25797506
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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