A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21504



Internal ID15840046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28595944..28597123hg38UCSC Ensembl
Outerchr15:28595338..28597562hg38UCSC Ensembl
Innerchr15:28841090..28842269hg19UCSC Ensembl
Outerchr15:28840484..28842708hg19UCSC Ensembl
Innerchr15:26640131..26641310hg18UCSC Ensembl
Outerchr15:26639525..26641749hg18UCSC Ensembl
Innerchr15:26640131..26641310hg17UCSC Ensembl
Outerchr15:26639525..26641749hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382225
hg192225
hg182225
hg172225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA18975
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)nssv21504
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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