A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3577886

Internal ID18359398
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59516357..59526296hg38UCSC Ensembl
Innerchr1:59982029..59991968hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv41e212
Supporting Variantsessv9767489, essv9767411, essv9767400, essv9767467, essv9767511, essv9767500, essv9767423, essv9767478, essv9767389, essv9767445, essv9767456, essv9767434
Samples401571SD, 401818PC, 400927BD, 401281BP, 402033WD, 402038MR, 400051MR, 400236DB, 401700BN, 401235IA, 401415CB, 400468OB
Known GenesFGGY
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
Pubmed ID25503493
Accession Number(s)esv3577886
Sample Size873
Observed Gain0
Observed Loss12
Observed Complex0

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