A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10022



Internal ID15844985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18532698..18546942hg38UCSC Ensembl
OuterchrY:20694584..20708828hg19UCSC Ensembl
OuterchrY:19153972..19168216hg18UCSC Ensembl
OuterchrY:19082709..19096953hg17UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3814245
hg1914245
hg1814245
hg1714245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27885
SamplesNA18504
Known GenesHSFY1, HSFY2
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)nsv10022
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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