A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26008



Internal ID15841692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91376599..91377981hg38UCSC Ensembl
Outerchr15:91375395..91378666hg38UCSC Ensembl
Innerchr15:91919829..91921211hg19UCSC Ensembl
Outerchr15:91918625..91921896hg19UCSC Ensembl
Innerchr15:89720833..89722215hg18UCSC Ensembl
Outerchr15:89719629..89722900hg18UCSC Ensembl
Innerchr15:89720833..89722215hg17UCSC 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 StatusS
Merged Variantsnsv9297
Supporting Variants
SamplesNA19132
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)nssv26008
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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