A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25630



Internal ID15481002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21878796..21916159hg38UCSC Ensembl
OuterchrY:21876956..21916220hg38UCSC Ensembl
InnerchrY:24024943..24062306hg19UCSC Ensembl
OuterchrY:24023103..24062367hg19UCSC Ensembl
InnerchrY:22434331..22471694hg18UCSC Ensembl
OuterchrY:22432491..22471755hg18UCSC Ensembl
InnerchrY:22363068..22400431hg17UCSC Ensembl
OuterchrY:22361228..22400492hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3839265
hg1939265
hg1839265
hg1739265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA07029
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)nssv25630
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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