A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10017



Internal ID15844980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10028347..10029705hg38UCSC Ensembl
OuterchrY:9865956..9867314hg19UCSC Ensembl
OuterchrY:10475956..10477314hg18UCSC Ensembl
OuterchrY:10459317..10460675hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg381359
hg191359
hg181359
hg171359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27595
SamplesNA12155
Known Genes
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)nsv10017
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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