A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2761448



Internal ID10374246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89825402..89841758hg38UCSC Ensembl
Innerchr8:90837630..90853986hg19UCSC Ensembl
Innerchr8:90906777..90923153hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3816357
hg1916357
hg1816377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6993259
SamplesSW_1480
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)esv2761448
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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