A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7004490



Internal ID10018220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16384236..16981773hg38UCSC Ensembl
Innerchr22:16864898..17462663hg19UCSC Ensembl
Innerchr22:15244898..15842663hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38597538
hg19597766
hg18597766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2763696
Supporting Variants
SamplesSW_1119
Known GenesANKRD62P1-PARP4P3, CCT8L2, GAB4, HSFY1P1, TPTEP1, XKR3
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)essv7004490
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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