A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9284



Internal ID15500510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82351990..82396777hg38UCSC Ensembl
Outerchr15:82644219..82688988hg19UCSC Ensembl
Outerchr15:80431274..80476043hg18UCSC Ensembl
Outerchr15:80431274..80476043hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3844788
hg1944770
hg1844770
hg1744770
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22066, nssv20381, nssv26298, nssv24545, nssv19895, nssv21903
SamplesNA18504, NA18860, NA07048, NA10847, NA12872, NA18552
Known GenesUBE2Q2P2, UBE2Q2P3
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)nsv9284
Frequency
Sample Size31
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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