A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10669



Internal ID15845632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:13195328..13338913hg38UCSC Ensembl
Outerchr5:13195440..13339025hg19UCSC Ensembl
Outerchr5:13248440..13392025hg18UCSC Ensembl
Outerchr5:13248440..13392025hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38143586
hg19143586
hg18143586
hg17143586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15233, nssv12636
SamplesNA10863, NA18972
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)nsv10669
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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