A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7004466



Internal ID10006966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15570064..15875621hg38UCSC Ensembl
Innerchr22:16102342..16407899hg19UCSC Ensembl
Innerchr22:14482342..14787899hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38305558
hg19305558
hg18305558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763707
Supporting Variants
SamplesSW_0120
Known GenesBMS1P17, BMS1P18, POTEH
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)essv7004466
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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