A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9296



Internal ID15847208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90246883..90249287hg38UCSC Ensembl
Outerchr15:90790115..90792519hg19UCSC Ensembl
Outerchr15:88591119..88593523hg18UCSC Ensembl
Outerchr15:88591119..88593523hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382405
hg192405
hg182405
hg172405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25988
SamplesNA19132
Known GenesCIB1
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)nsv9296
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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