A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787641



Internal ID18814070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15545427..15573966hg38UCSC Ensembl
Innerchr8:15402936..15431475hg19UCSC Ensembl
Innerchr8:15447307..15475846hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3828540
hg1928540
hg1828540
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 550
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787641
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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