A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9255



Internal ID15847167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43843954..43849428hg38UCSC Ensembl
Outerchr15:44136152..44141626hg19UCSC Ensembl
Outerchr15:41923444..41928918hg18UCSC Ensembl
Outerchr15:41923444..41928918hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg385475
hg195475
hg185475
hg175475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23571, nssv21813
SamplesNA12155, NA07048
Known GenesWDR76
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)nsv9255
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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