A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833127



Internal ID6158851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3202782..3309413hg19UCSC Ensembl
Outerchr16:3142783..3249414hg18UCSC Ensembl
Outerchr16:3142783..3249414hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain+Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1452249, nssv1452254, nssv1452250, nssv1452252, nssv1452253, nssv1452255, nssv1452251
Samples
Known GenesMEFV, OR1F1, OR1F2P, ZNF200
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833127
Frequency
Sample Size95
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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