A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577960



Internal ID18706158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72542484..72620518hg38UCSC Ensembl
Innerchr1:73008167..73086201hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3878035
hg1978035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv54e212
Supporting Variantsessv9774133
Samples401292ER
Known Genes
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)esv3577960
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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