A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2762760



Internal ID10375558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100733333..100756447hg38UCSC Ensembl
Innerchr8:101745561..101768675hg19UCSC Ensembl
Innerchr8:101814737..101837851hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3823115
hg1923115
hg1823115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7017073
SamplesRW_0227
Known Genes
MethodMerging
AnalysisTwo different algorithms (PennCNV and Birdseye) were applied to detect CNVs. Only congruent CNV events regarding direction of effect that were detected by both algorithms were merged using the outer borders of the event in a first step. In a second step only CNVs that were detected in at least two individuals were merged into a CNVR.
PlatformMerging
Comments
ReferenceVogler_et_al_2010
Pubmed ID21179565
Accession Number(s)esv2762760
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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