A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10478



Internal ID15845441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34437128..34451410hg38UCSC Ensembl
Outerchr4:34438750..34453032hg19UCSC Ensembl
Outerchr4:34115145..34129427hg18UCSC Ensembl
Outerchr4:34261316..34275598hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3814283
hg1914283
hg1814283
hg1714283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13032
SamplesNA18502
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)nsv10478
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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