A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv751e212



Internal ID20149207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81149203..81171619hg38UCSC Ensembl
chr15:81441544..81463960hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3822417
hg1922417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3581783, esv3581785, esv3581784
Samples401852SK, 400268SY, 400789KV, 400014SL, 400818BL, 400654YW, 401894PD, 400266BA
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)dgv751e212
Frequency
Sample Size873
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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