A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26581



Internal ID15836040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22167263..22181074hg38UCSC Ensembl
OuterchrY:22165449..22181135hg38UCSC Ensembl
InnerchrY:24313410..24327221hg19UCSC Ensembl
OuterchrY:24311596..24327282hg19UCSC Ensembl
InnerchrY:22722798..22736609hg18UCSC Ensembl
OuterchrY:22720984..22736670hg18UCSC Ensembl
InnerchrY:22651535..22665346hg17UCSC Ensembl
OuterchrY:22649721..22665407hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3815687
hg1915687
hg1815687
hg1715687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10029
Supporting Variants
SamplesNA18563
Known GenesRBMY1F, RBMY1J
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)nssv26581
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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