A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7004196



Internal ID10362357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59722413..59740559hg38UCSC Ensembl
Innerchr20:58297468..58315614hg19UCSC Ensembl
Innerchr20:57730863..57749009hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3818147
hg1918147
hg1818147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763668
Supporting Variants
SamplesSW_1033
Known GenesPHACTR3
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)essv7004196
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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