A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv28366



Internal ID15491640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:23265719..23280518hg38UCSC Ensembl
OuterchrY:23265480..23281310hg38UCSC Ensembl
InnerchrY:25411866..25426665hg19UCSC Ensembl
OuterchrY:25411627..25427457hg19UCSC Ensembl
InnerchrY:23821254..23836053hg18UCSC Ensembl
OuterchrY:23821015..23836845hg18UCSC Ensembl
InnerchrY:23749991..23764790hg17UCSC Ensembl
OuterchrY:23749752..23765582hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3815831
hg1915831
hg1815831
hg1715831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10034
Supporting Variants
SamplesNA18860
Known GenesDAZ2, DAZ3, DAZ4
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)nssv28366
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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