A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526186



Internal ID6021788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42676481..43203507hg19UCSC Ensembl
Innerchr19:47368321..47895347hg18UCSC Ensembl
Innerchr19:47368321..47895347hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv702448
Samples
Known GenesCEACAM1, CEACAM8, CIC, CNFN, CXCL17, DEDD2, ERF, GSK3A, LIPE, MEGF8, PAFAH1B3, PRR19, TMEM145, ZNF526
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv526186
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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