A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784977



Internal ID18824761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545789..15574673hg38UCSC Ensembl
Innerchr8:15403298..15432182hg19UCSC Ensembl
Innerchr8:15447669..15476553hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3828885
hg1928885
hg1828885
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891353
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784977
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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