A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24149



Internal ID15484669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89574453..89575054hg38UCSC Ensembl
Outerchr16:89573333..89577040hg38UCSC Ensembl
Innerchr16:89640861..89641462hg19UCSC Ensembl
Outerchr16:89639741..89643448hg19UCSC Ensembl
Innerchr16:88168362..88168963hg18UCSC Ensembl
Outerchr16:88167242..88170949hg18UCSC Ensembl
Innerchr16:88168362..88168963hg17UCSC Ensembl
Outerchr16:88167242..88170949hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383708
hg193708
hg183708
hg173708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9477
Supporting Variants
SamplesNA12740
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)nssv24149
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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