A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9362



Internal ID15500588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:16291038..16292215hg38UCSC Ensembl
Outerchr16:16384895..16386072hg19UCSC Ensembl
Outerchr16:16292396..16293573hg18UCSC Ensembl
Outerchr16:16292396..16293573hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381178
hg191178
hg181178
hg171178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23894, nssv23507
SamplesNA19173, NA19144
Known GenesNOMO3
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)nsv9362
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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