A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9951



Internal ID15847863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:71653082..71697349hg38UCSC Ensembl
OuterchrX:70872932..70917199hg19UCSC Ensembl
OuterchrX:70789657..70833924hg18UCSC Ensembl
OuterchrX:70655953..70700220hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3844268
hg1944268
hg1844268
hg1744268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27533
SamplesNA18504
Known GenesBCYRN1, LINC00891, LOC100132741
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)nsv9951
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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