A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23431



Internal ID15483876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32154307..32387870hg38UCSC Ensembl
Outerchr15:32153679..32389318hg38UCSC Ensembl
Innerchr15:32446508..32680071hg19UCSC Ensembl
Outerchr15:32445880..32681519hg19UCSC Ensembl
Innerchr15:30233800..30467363hg18UCSC Ensembl
Outerchr15:30233172..30468811hg18UCSC Ensembl
Innerchr15:30233800..30467363hg17UCSC Ensembl
Outerchr15:30233172..30468811hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38235640
hg19235640
hg18235640
hg17235640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA12155
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)nssv23431
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer