A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2763608



Internal ID10030958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163499085..163522397hg38UCSC Ensembl
Innerchr6:163920117..163943429hg19UCSC Ensembl
Innerchr6:163840107..163863419hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3823313
hg1923313
hg1823313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7033250
SamplesSW_0016
Known GenesQKI
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)esv2763608
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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