A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27565



Internal ID15833576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:71785478..71789273hg38UCSC Ensembl
OuterchrX:71784760..71789563hg38UCSC Ensembl
InnerchrX:71005328..71009123hg19UCSC Ensembl
OuterchrX:71004610..71009413hg19UCSC Ensembl
InnerchrX:70922053..70925848hg18UCSC Ensembl
OuterchrX:70921335..70926138hg18UCSC Ensembl
InnerchrX:70788349..70792144hg17UCSC Ensembl
OuterchrX:70787631..70792434hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg384804
hg194804
hg184804
hg174804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9955
Supporting Variants
SamplesNA18504
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)nssv27565
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer