A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577856



Internal ID18706054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:53122791..53130294hg38UCSC Ensembl
Innerchr1:53588463..53595966hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg387504
hg197504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9836277, essv9836288
Samples401196CR, 401732HW
Known GenesSLC1A7
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)esv3577856
Frequency
Sample Size873
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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