A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25268



Internal ID15483739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89570567..89604827hg38UCSC Ensembl
Outerchr16:89569883..89608647hg38UCSC Ensembl
Innerchr16:89636975..89671235hg19UCSC Ensembl
Outerchr16:89636291..89675055hg19UCSC Ensembl
Innerchr16:88164476..88198736hg18UCSC Ensembl
Outerchr16:88163792..88202556hg18UCSC Ensembl
Innerchr16:88164476..88198736hg17UCSC Ensembl
Outerchr16:88163792..88202556hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3838765
hg1938765
hg1838765
hg1738765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9477
Supporting Variants
SamplesNA12155
Known GenesCPNE7
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)nssv25268
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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