A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891429



Internal ID19185825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85557959..85601185hg38UCSC Ensembl
Outerchr8:85556121..85617541hg38UCSC Ensembl
Innerchr8:86470188..86513414hg19UCSC Ensembl
Outerchr8:86468350..86529770hg19UCSC Ensembl
Innerchr8:86657440..86700666hg18UCSC Ensembl
Outerchr8:86655602..86717022hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3861421
hg1961421
hg1861421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782121, essv25779084, essv25779289, essv25801497, essv25779004, essv25797194, essv25779214
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891429
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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