A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27903



Internal ID15486978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21491816..21917792hg38UCSC Ensembl
OuterchrY:21491074..21918190hg38UCSC Ensembl
InnerchrY:23653702..24063939hg19UCSC Ensembl
OuterchrY:23652960..24064337hg19UCSC Ensembl
InnerchrY:22063090..22473327hg18UCSC Ensembl
OuterchrY:22062348..22473725hg18UCSC Ensembl
InnerchrY:21991827..22402064hg17UCSC Ensembl
OuterchrY:21991085..22402462hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38427117
hg19411378
hg18411378
hg17411378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA18504
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E, TTTY13
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)nssv27903
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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