A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778726



Internal ID19165719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68955731..69264211hg38UCSC Ensembl
Innerchr4:69821449..70129929hg19UCSC Ensembl
Innerchr4:69856038..70164518hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38308481
hg19308481
hg18308481
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893952
Supporting Variants
Samples
Known GenesUGT2B10, UGT2B11, UGT2B7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=81
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778726
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