A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21202



Internal ID15492144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32235445..32240631hg38UCSC Ensembl
Outerchr16:32235339..32241521hg38UCSC Ensembl
Innerchr16:32246766..32251952hg19UCSC Ensembl
Outerchr16:32246660..32252842hg19UCSC Ensembl
Innerchr16:32154267..32159453hg18UCSC Ensembl
Outerchr16:32154161..32160343hg18UCSC Ensembl
Innerchr16:32154267..32159453hg17UCSC Ensembl
Outerchr16:32154161..32160343hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386183
hg196183
hg186183
hg176183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18942
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)nssv21202
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer