A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7026663



Internal ID9996460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21461577..21490778hg38UCSC Ensembl
Innerchr22:21815866..21845067hg19UCSC Ensembl
Innerchr22:20145866..20175067hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3829202
hg1929202
hg1829202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2760719
Supporting Variants
SamplesRW_0289
Known GenesPI4KAP2, TMEM191C
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)essv7026663
Frequency
Sample Size1109
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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