A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891456



Internal ID19185852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106860349..106881249hg38UCSC Ensembl
Outerchr8:106860349..106881249hg38UCSC Ensembl
Innerchr8:107872577..107893477hg19UCSC Ensembl
Outerchr8:107872577..107893477hg19UCSC Ensembl
Innerchr8:107941753..107962653hg18UCSC Ensembl
Outerchr8:107941753..107962653hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3820901
hg1920901
hg1820901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779472
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891456
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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