A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891354



Internal ID19185750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15565155..15678207hg38UCSC Ensembl
Outerchr8:15565155..15678207hg38UCSC Ensembl
Innerchr8:15422664..15535716hg19UCSC Ensembl
Outerchr8:15422664..15535716hg19UCSC Ensembl
Innerchr8:15467035..15580087hg18UCSC Ensembl
Outerchr8:15467035..15580087hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38113053
hg19113053
hg18113053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779045
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891354
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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