A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9239



Internal ID15500465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:32619146..32633201hg38UCSC Ensembl
Outerchr15:32911347..32925402hg19UCSC Ensembl
Outerchr15:30698639..30712694hg18UCSC Ensembl
Outerchr15:30698639..30712694hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3814056
hg1914056
hg1814056
hg1714056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23542
SamplesNA11830
Known GenesARHGAP11A
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)nsv9239
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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