A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10471



Internal ID15845434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:29224761..29240322hg38UCSC Ensembl
Outerchr4:29226383..29241944hg19UCSC Ensembl
Outerchr4:28835481..28851042hg18UCSC Ensembl
Outerchr4:28902652..28918213hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3815562
hg1915562
hg1815562
hg1715562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11935, nssv13017, nssv12391
SamplesNA18980, NA19132, NA19240
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)nsv10471
Frequency
Sample Size31
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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