A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23402



Internal ID15829959
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
hg38n/a
hg19429942
hg18n/a
hg17n/a
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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