A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9297



Internal ID15847209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91375395..91378666hg38UCSC Ensembl
Outerchr15:91918625..91921896hg19UCSC Ensembl
Outerchr15:89719629..89722900hg18UCSC Ensembl
Outerchr15:89719629..89722900hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383272
hg193272
hg183272
hg173272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22616, nssv26008
SamplesNA19007, NA19132
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)nsv9297
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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