A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784132



Internal ID18821565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38798089..38819365hg38UCSC Ensembl
Innerchr4:38799710..38820986hg19UCSC Ensembl
Innerchr4:38476105..38497381hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3821277
hg1921277
hg1821277
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893918
Supporting Variants
Samples
Known GenesTLR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784132
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