A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22974



Internal ID15481395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33805715..33823496hg38UCSC Ensembl
Outerchr16:33805417..33825259hg38UCSC Ensembl
Innerchr16:33608182..33625963hg19UCSC Ensembl
Outerchr16:33607884..33627726hg19UCSC Ensembl
Innerchr16:33515683..33533464hg18UCSC Ensembl
Outerchr16:33515385..33535227hg18UCSC Ensembl
Innerchr16:33515683..33533464hg17UCSC Ensembl
Outerchr16:33515385..33535227hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3819843
hg1919843
hg1819843
hg1719843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA07048
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)nssv22974
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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