A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7026599



Internal ID9990092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15832401..15925481hg38UCSC Ensembl
Innerchr22:16052528..16145562hg19UCSC Ensembl
Innerchr22:14432528..14525562hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3893081
hg1993035
hg1893035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760727
Supporting Variants
SamplesRW_0138
Known Genes
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)essv7026599
Frequency
Sample Size1109
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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