A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22733



Internal ID15494148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:690961..700518hg38UCSC Ensembl
Outerchr16:690468..701168hg38UCSC Ensembl
Innerchr16:740961..750518hg19UCSC Ensembl
Outerchr16:740468..751168hg19UCSC Ensembl
Innerchr16:680962..690519hg18UCSC Ensembl
Outerchr16:680469..691169hg18UCSC Ensembl
Innerchr16:680962..690519hg17UCSC Ensembl
Outerchr16:680469..691169hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810701
hg1910701
hg1810701
hg1710701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9321
Supporting Variants
SamplesNA18980
Known GenesFBXL16
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)nssv22733
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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