A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9338



Internal ID15847250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4164188..4167342hg38UCSC Ensembl
Outerchr16:4214189..4217343hg19UCSC Ensembl
Outerchr16:4154190..4157344hg18UCSC Ensembl
Outerchr16:4154190..4157344hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383155
hg193155
hg183155
hg173155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23840
SamplesNA19144
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)nsv9338
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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