A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8684



Internal ID15846596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:68744716..68749667hg38UCSC Ensembl
Outerchr10:70504473..70509424hg19UCSC Ensembl
Outerchr10:70174479..70179430hg18UCSC Ensembl
Outerchr10:70174479..70179430hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384952
hg194952
hg184952
hg174952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21854
SamplesNA18517
Known GenesCCAR1
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)nsv8684
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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