A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23277



Internal ID15494220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32855995..33024570hg38UCSC Ensembl
Outerchr16:32855764..33025396hg38UCSC Ensembl
Innerchr16:32867316..33035891hg19UCSC Ensembl
Outerchr16:32867085..33036717hg19UCSC Ensembl
Innerchr16:32774817..32943392hg18UCSC Ensembl
Outerchr16:32774586..32944218hg18UCSC Ensembl
Innerchr16:32774817..32943392hg17UCSC Ensembl
Outerchr16:32774586..32944218hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38169633
hg19169633
hg18169633
hg17169633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18980
Known GenesSLC6A10P
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)nssv23277
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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