A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25377



Internal ID15837413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:15712867..15715934hg38UCSC Ensembl
Outerchr22:15712598..15716126hg38UCSC Ensembl
Innerchr22:16262029..16265096hg19UCSC Ensembl
Outerchr22:16261837..16265365hg19UCSC Ensembl
Innerchr22:14642029..14645096hg18UCSC Ensembl
Outerchr22:14641837..14645365hg18UCSC Ensembl
Innerchr22:14642029..14645096hg17UCSC Ensembl
Outerchr22:14641837..14645365hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg383529
hg193529
hg183529
hg173529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9866
Supporting Variants
SamplesNA18853
Known GenesPOTEH
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)nssv25377
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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