A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3577083



Internal ID18705281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47078813..47692945hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19614133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv220e212
Supporting Variantsessv9793354
Samples400717BD
Known GenesAGAP9, ANTXRL, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
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)esv3577083
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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