A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24087



Internal ID15496658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33120583..33121086hg38UCSC Ensembl
Outerchr16:33119970..33121490hg38UCSC Ensembl
Innerchr16:33131904..33132407hg19UCSC Ensembl
Outerchr16:33131291..33132811hg19UCSC Ensembl
Innerchr16:33039405..33039908hg18UCSC Ensembl
Outerchr16:33038792..33040312hg18UCSC Ensembl
Innerchr16:33039405..33039908hg17UCSC Ensembl
Outerchr16:33038792..33040312hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381521
hg191521
hg181521
hg171521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19173
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)nssv24087
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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