A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9476



Internal ID15500702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89402153..89405691hg38UCSC Ensembl
Outerchr16:89468561..89472099hg19UCSC Ensembl
Outerchr16:87996062..87999600hg18UCSC Ensembl
Outerchr16:87996062..87999600hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383539
hg193539
hg183539
hg173539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26539
SamplesNA18972
Known GenesANKRD11
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)nsv9476
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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