A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891466



Internal ID19185862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115474215..115525606hg38UCSC Ensembl
Outerchr8:115474215..115525606hg38UCSC Ensembl
Innerchr8:116486442..116537833hg19UCSC Ensembl
Outerchr8:116486442..116537833hg19UCSC Ensembl
Innerchr8:116555618..116607008hg18UCSC Ensembl
Outerchr8:116555618..116607008hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3851392
hg1951392
hg1851391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784358
Samples
Known GenesTRPS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891466
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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