A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv28324



Internal ID15491461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21879085..21923586hg38UCSC Ensembl
OuterchrY:21878796..21924034hg38UCSC Ensembl
InnerchrY:24025232..24069733hg19UCSC Ensembl
OuterchrY:24024943..24070181hg19UCSC Ensembl
InnerchrY:22434620..22479121hg18UCSC Ensembl
OuterchrY:22434331..22479569hg18UCSC Ensembl
InnerchrY:22363357..22407858hg17UCSC Ensembl
OuterchrY:22363068..22408306hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3845239
hg1945239
hg1845239
hg1745239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10026
Supporting Variants
SamplesNA18860
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)nssv28324
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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