A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788837



Internal ID18823462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7432672..7854519hg38UCSC Ensembl
Innerchr8:7290194..7712041hg19UCSC Ensembl
Innerchr8:7277604..7749451hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38421848
hg19421848
hg18471848
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891321
Supporting Variants
Samples
Known GenesDEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788837
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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