A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23837



Internal ID15493951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89579443..89580196hg38UCSC Ensembl
Outerchr16:89578885..89581482hg38UCSC Ensembl
Innerchr16:89645851..89646604hg19UCSC Ensembl
Outerchr16:89645293..89647890hg19UCSC Ensembl
Innerchr16:88173352..88174105hg18UCSC Ensembl
Outerchr16:88172794..88175391hg18UCSC Ensembl
Innerchr16:88173352..88174105hg17UCSC Ensembl
Outerchr16:88172794..88175391hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382598
hg192598
hg182598
hg172598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9477
Supporting Variants
SamplesNA18980
Known GenesCPNE7
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)nssv23837
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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