A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25352



Internal ID15837515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15844044..15874258hg38UCSC Ensembl
Outerchr22:15843405..15874673hg38UCSC Ensembl
Innerchr22:16103705..16133919hg19UCSC Ensembl
Outerchr22:16103290..16134558hg19UCSC Ensembl
Innerchr22:14483705..14513919hg18UCSC Ensembl
Outerchr22:14483290..14514558hg18UCSC Ensembl
Innerchr22:14483705..14513919hg17UCSC Ensembl
Outerchr22:14483290..14514558hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3831269
hg1931269
hg1831269
hg1731269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9866
Supporting Variants
SamplesNA18853
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)nssv25352
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