A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891475



Internal ID19185871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121671200..121686649hg38UCSC Ensembl
Outerchr8:121671200..121686649hg38UCSC Ensembl
Innerchr8:122683440..122698889hg19UCSC Ensembl
Outerchr8:122683440..122698889hg19UCSC Ensembl
Innerchr8:122752621..122768070hg18UCSC Ensembl
Outerchr8:122752621..122768070hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3815450
hg1915450
hg1815450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780455
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891475
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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