A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797233



Internal ID18829360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177303484..177340740hg38UCSC Ensembl
Innerchr4:178224638..178261894hg19UCSC Ensembl
Innerchr4:178461632..178498888hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3837257
hg1937257
hg1837257
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894076
Supporting Variants
Samples
Known GenesNEIL3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797233
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