A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv1350e212

Internal ID20149806
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2445826..2447097hg38UCSC Ensembl
chr3:2487510..2488781hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3568556, esv3568557, esv3568554, esv3568555
Samples401017SC, 400888MS, 400782IE, 400130HA, 400949AM, 400800MW, 401275SJ, 401912HD, 400227MM, 401105WS, 400132HN, 401136LB, 401640WJ, 401721CP, 401966SR, 401566DD, 401836SI, 400246MG, 400106PC, 400093BL, 400821FE, 401326LI, 401636WR, 401487FW, 400893ZE, 401950MD, 400615RI, 401180GR, 400136DM, 400353ML, 401864CV, 400267GD, 401563TK, 402028BD, 400141CC, 400053LE, 401117NA, 401427CB, 400077EB, 400737GC, 400722OM, 401540NA, 400728PB, 400739SS, 400704LC, 400177CG, 400763BT, 401496SL, 400148MS, 400236DB, 401365DJ, 400825TW, 400006DK, 401053MF, 401634CH, 401913GT, 400769SL, 400639RP, 400645KM, 401889FR, 400156WT, 401813DN, 401908YM, 400340CD
Known GenesCNTN4
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)dgv1350e212
Sample Size873
Observed Gain0
Observed Loss64
Observed Complex0

Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer