A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9288



Internal ID15847200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82810732..82828076hg38UCSC Ensembl
Outerchr15:83479484..83496828hg19UCSC Ensembl
Outerchr15:81276538..81293882hg18UCSC Ensembl
Outerchr15:81276538..81293882hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3817345
hg1917345
hg1817345
hg1717345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25895
SamplesNA19132
Known GenesWHAMM
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)nsv9288
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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