A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7026637



Internal ID10000564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15602991..15772197hg38UCSC Ensembl
Innerchr22:16205766..16374972hg19UCSC Ensembl
Innerchr22:14585766..14754972hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38169207
hg19169207
hg18169207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760727
Supporting Variants
SamplesRW_0558
Known GenesPOTEH
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)essv7026637
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer