A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25663



Internal ID15836205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15888703..15915813hg38UCSC Ensembl
Outerchr22:15888370..15916723hg38UCSC Ensembl
Innerchr22:16062144..16089260hg19UCSC Ensembl
Outerchr22:16061234..16089593hg19UCSC Ensembl
Innerchr22:14442144..14469260hg18UCSC Ensembl
Outerchr22:14441234..14469593hg18UCSC Ensembl
Innerchr22:14442144..14469260hg17UCSC Ensembl
Outerchr22:14441234..14469593hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3828354
hg1928360
hg1828360
hg1728360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9866
Supporting Variants
SamplesNA18563
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)nssv25663
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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