A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22266



Internal ID15482810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32378903..32386936hg38UCSC Ensembl
Outerchr16:32364217..32387262hg38UCSC Ensembl
Innerchr16:32390224..32398257hg19UCSC Ensembl
Outerchr16:32375538..32398583hg19UCSC Ensembl
Innerchr16:32297725..32305758hg18UCSC Ensembl
Outerchr16:32283039..32306084hg18UCSC Ensembl
Innerchr16:32297725..32305758hg17UCSC Ensembl
Outerchr16:32283039..32306084hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3823046
hg1923046
hg1823046
hg1723046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA10863
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)nssv22266
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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