A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891330



Internal ID19185726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9181086..9255062hg38UCSC Ensembl
Outerchr8:9178319..9309665hg38UCSC Ensembl
Innerchr8:9038596..9112572hg19UCSC Ensembl
Outerchr8:9035829..9167175hg19UCSC Ensembl
Innerchr8:9076006..9149982hg18UCSC Ensembl
Outerchr8:9073239..9204585hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38131347
hg19131347
hg18131347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797350, essv25782322
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891330
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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