A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577661



Internal ID18705859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26193788..26277350hg38UCSC Ensembl
InnerchrY:28339935..28423497hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3883563
hg1983563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2582e212
Supporting Variantsessv9834602
Samples400620MT
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)esv3577661
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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