A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27641



Internal ID15483935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21875268..21926258hg38UCSC Ensembl
OuterchrY:21875132..21926287hg38UCSC Ensembl
InnerchrY:24021415..24072405hg19UCSC Ensembl
OuterchrY:24021279..24072434hg19UCSC Ensembl
InnerchrY:22430803..22481793hg18UCSC Ensembl
OuterchrY:22430667..22481822hg18UCSC Ensembl
InnerchrY:22359540..22410530hg17UCSC Ensembl
OuterchrY:22359404..22410559hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3851156
hg1951156
hg1851156
hg1751156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA12155
Known GenesRBMY1A1, RBMY1B, RBMY1D, RBMY1E
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)nssv27641
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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