A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894004



Internal ID19184858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110063399..110076619hg38UCSC Ensembl
Outerchr4:110063399..110076619hg38UCSC Ensembl
Innerchr4:110984555..110997775hg19UCSC Ensembl
Outerchr4:110984555..110997775hg19UCSC Ensembl
Innerchr4:111204004..111217224hg18UCSC Ensembl
Outerchr4:111204004..111217224hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3813221
hg1913221
hg1813221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785250, essv25780442
Samples
Known GenesELOVL6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894004
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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