A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7026921



Internal ID10001851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25526375..25602486hg38UCSC Ensembl
Innerchr22:25922342..25998453hg19UCSC Ensembl
Innerchr22:24252342..24328453hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3876112
hg1976112
hg1876112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760720
Supporting Variants
SamplesRW_0593
Known GenesADRBK2
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)essv7026921
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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