A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23262



Internal ID15831269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19494..31285hg38UCSC Ensembl
Outerchr16:17571..31856hg38UCSC Ensembl
Innerchr16:69494..81285hg19UCSC Ensembl
Outerchr16:67571..81856hg19UCSC Ensembl
Innerchr16:9494..21285hg18UCSC Ensembl
Outerchr16:7571..21856hg18UCSC Ensembl
Innerchr16:9494..21285hg17UCSC Ensembl
Outerchr16:7571..21856hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814286
hg1914286
hg1814286
hg1714286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9316
Supporting Variants
SamplesNA12740
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)nssv23262
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