A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24455



Internal ID15495580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33807427..33825995hg38UCSC Ensembl
Outerchr16:33805715..33826664hg38UCSC Ensembl
Innerchr16:33609894..33628462hg19UCSC Ensembl
Outerchr16:33608182..33629131hg19UCSC Ensembl
Innerchr16:33517395..33535963hg18UCSC Ensembl
Outerchr16:33515683..33536632hg18UCSC Ensembl
Innerchr16:33517395..33535963hg17UCSC Ensembl
Outerchr16:33515683..33536632hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820950
hg1920950
hg1820950
hg1720950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
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)nssv24455
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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