A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23402



Internal ID15483273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31724189..32153024hg38UCSC Ensembl
Outerchr15:31723736..32153679hg38UCSC Ensembl
Innerchr15:32016392..32445225hg19UCSC Ensembl
Outerchr15:32015939..32445880hg19UCSC Ensembl
Innerchr15:29803684..30232517hg18UCSC Ensembl
Outerchr15:29803231..30233172hg18UCSC Ensembl
Innerchr15:29803684..30232517hg17UCSC Ensembl
Outerchr15:29803231..30233172hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38429944
hg19429942
hg18429942
hg17429942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9237
Supporting Variants
SamplesNA11830
Known GenesCHRNA7
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)nssv23402
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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