A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10262



Internal ID15498539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:37860290..37863364hg38UCSC Ensembl
Outerchr3:37901781..37904855hg19UCSC Ensembl
Outerchr3:37876785..37879859hg18UCSC Ensembl
Outerchr3:37876785..37879859hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg383075
hg193075
hg183075
hg173075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11832
SamplesNA18502
Known GenesCTDSPL
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)nsv10262
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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