A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9224



Internal ID15500450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28947412..28949055hg38UCSC Ensembl
Outerchr15:29239615..29241258hg19UCSC Ensembl
Outerchr15:27026907..27028550hg18UCSC Ensembl
Outerchr15:27026907..27028550hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381644
hg191644
hg181644
hg171644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26044
SamplesNA18860
Known GenesAPBA2
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)nsv9224
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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