A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9933



Internal ID15847845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9401300..9414810hg38UCSC Ensembl
OuterchrX:9369340..9382850hg19UCSC Ensembl
OuterchrX:9329340..9342850hg18UCSC Ensembl
OuterchrX:9179076..9192586hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3813511
hg1913511
hg1813511
hg1713511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26515, nssv27428, nssv27495, nssv25848, nssv23355, nssv28180, nssv26247, nssv26830, nssv26118
SamplesNA18504, NA12155, NA18563, NA18860, NA19007, NA18572, NA18853, NA19144, NA19173
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)nsv9933
Frequency
Sample Size31
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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