A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10277



Internal ID15498554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:62725415..62731442hg38UCSC Ensembl
Outerchr3:62711090..62717117hg19UCSC Ensembl
Outerchr3:62686130..62692157hg18UCSC Ensembl
Outerchr3:62686130..62692157hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg386028
hg196028
hg186028
hg176028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28825
SamplesNA19144
Known GenesCADPS
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)nsv10277
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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