A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21854



Internal ID15834253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68747598..68749062hg38UCSC Ensembl
Outerchr10:68744716..68749667hg38UCSC Ensembl
Innerchr10:70507355..70508819hg19UCSC Ensembl
Outerchr10:70504473..70509424hg19UCSC Ensembl
Innerchr10:70177361..70178825hg18UCSC Ensembl
Outerchr10:70174479..70179430hg18UCSC Ensembl
Innerchr10:70177361..70178825hg17UCSC 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 StatusS
Merged Variantsnsv8684
Supporting Variants
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)nssv21854
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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