A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3568283



Internal ID18349795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21685588..21699487hg38UCSC Ensembl
Innerchr22:22039877..22053776hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1293e212
Supporting Variantsessv9821215, essv9821246, essv9821230, essv9821223, essv9821249, essv9821214, essv9821251, essv9821250, essv9821241, essv9821213, essv9821245, essv9821235, essv9821207, essv9821247, essv9821228, essv9821221, essv9821237, essv9821234, essv9821216, essv9821208, essv9821220, essv9821217, essv9821219, essv9821238, essv9821239, essv9821224, essv9821206, essv9821226, essv9821212, essv9821248, essv9821242, essv9821231, essv9821209, essv9821229, essv9821232, essv9821240, essv9821227, essv9821210, essv9821218, essv9821243, essv9821225, essv9821236
Samples400063BR, 401212HJ, 400114GR, 40031BA, 401927SK, 400199SA, 401824MM, 401355CD, 400379BB, 401634CH, 401281BP, 401006ES, 401620BA, 400218WK, 400577MK, 401726LW, 400038CK, 400416KA, 401026AM, 401694SG, 401804FG, 401519SA, 400082SD, 401326LI, 400265LK, 401506LK, 401892MJ, 400639RP, 400524NJ, 401200BD, 400571WV, 400721DJ, 400671PP, 400542EG, 401898DS, 401847RK, 401010HT, 401143LK, 401056TJ, 401372RR, 400177SJ, 401362ME
Known GenesPPIL2, YPEL1
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3568283
Frequency
Sample Size873
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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