A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10025



Internal ID15498302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18865177..20859250hg38UCSC Ensembl
OuterchrY:21027063..23021136hg19UCSC Ensembl
OuterchrY:19486451..21430524hg18UCSC Ensembl
OuterchrY:19415188..21359261hg17UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg381994074
hg191994074
hg181944074
hg171944074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27897
SamplesNA18504
Known GenesBCORP1, CD24, EIF1AY, KDM5D, NCRNA00185, RPS4Y2, TTTY10, TTTY14, TXLNG2P
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)nsv10025
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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