A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796199



Internal ID19169327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:83170291..83202545hg38UCSC Ensembl
Innerchr4:84091444..84123698hg19UCSC Ensembl
Innerchr4:84310468..84342722hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3832255
hg1932255
hg1832255
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893972
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796199
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