A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9303



Internal ID15847215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:97553913..97559040hg38UCSC Ensembl
Outerchr15:98097143..98102270hg19UCSC Ensembl
Outerchr15:95898147..95903274hg18UCSC Ensembl
Outerchr15:95898147..95903274hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385128
hg195128
hg185128
hg175128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26133
SamplesNA18502
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)nsv9303
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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