A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9265



Internal ID15847177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51327401..51331034hg38UCSC Ensembl
Outerchr15:51619598..51623231hg19UCSC Ensembl
Outerchr15:49406890..49410523hg18UCSC Ensembl
Outerchr15:49406890..49410523hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383634
hg193634
hg183634
hg173634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22526, nssv20029
SamplesNA19007, NA18572
Known GenesCYP19A1
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)nsv9265
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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