A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891352



Internal ID19185748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15562268..15573966hg38UCSC Ensembl
Outerchr8:15562268..15574673hg38UCSC Ensembl
Innerchr8:15419777..15431475hg19UCSC Ensembl
Outerchr8:15419777..15432182hg19UCSC Ensembl
Innerchr8:15464148..15475846hg18UCSC Ensembl
Outerchr8:15464148..15476553hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3812406
hg1912406
hg1812406
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785950, essv25799056, essv25782993, essv25797774, essv25797307, essv25791519, essv25801596
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891352
Frequency
Sample Size3017
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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