A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10255



Internal ID15845218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:24787755..24791067hg38UCSC Ensembl
Outerchr3:24829246..24832558hg19UCSC Ensembl
Outerchr3:24804250..24807562hg18UCSC Ensembl
Outerchr3:24804250..24807562hg17UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg383313
hg193313
hg183313
hg173313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11983
SamplesNA18504
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)nsv10255
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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