A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1577e212



Internal ID22784504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9897855..9929804hg38UCSC Ensembl
chr5:9897967..9929916hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3831950
hg1931950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3569972, esv3569969, esv3569973, esv3569971, esv3569968, esv3569970
Samples401474CE, 400821FE, 401719RL, 400595CP, 401918CA, 400453LN, 402064DC, 401406KF, 401377MA, 401274PA, 400732MA, 401012TP, 402008MC, 400138LA
Known GenesLOC285692
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)dgv1577e212
Frequency
Sample Size873
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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