A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1926



Internal ID5089013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88692698..88726952hg19UCSC Ensembl
Outerchr16:87220199..87254453hg18UCSC Ensembl
Outerchr16:87220199..87254453hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg195748
hg185748
hg175748
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv2958
SamplesNA18555
Known GenesCYBA, IL17C, MVD, ZC3H18
Method
AnalysisSample level sites were merged to generate a set of non-redundant variant regions. Two non-redundant inversion variants (chr 2 positions 89438708-89655419 and 89958869-91208466) were corrected from the original publication for coordinates and associated sample-level data.
PlatformCapillary
Comments
ReferenceKidd et al 2008
Pubmed ID18451855
Accession Number(s)nsv1926
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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