A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23966



Internal ID15836880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:9897088..9908834hg38UCSC Ensembl
OuterchrY:9894559..9909819hg38UCSC Ensembl
InnerchrY:9734697..9746443hg19UCSC Ensembl
OuterchrY:9732168..9747428hg19UCSC Ensembl
InnerchrY:10344697..10356443hg18UCSC Ensembl
OuterchrY:10342168..10357428hg18UCSC Ensembl
InnerchrY:10328058..10339804hg17UCSC Ensembl
OuterchrY:10325529..10340789hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815261
hg1915261
hg1815261
hg1715261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10016
Supporting Variants
SamplesNA18572
Known Genes
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)nssv23966
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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