A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9420



Internal ID15847332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28779385..28813501hg38UCSC Ensembl
Outerchr16:28790706..28824822hg19UCSC Ensembl
Outerchr16:28698207..28732323hg18UCSC Ensembl
Outerchr16:28698207..28732323hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3834117
hg1934117
hg1834117
hg1734117
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24013, nssv22254
SamplesNA11830, NA18975
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv9420
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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