A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26529



Internal ID15843330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:67908666..67910302hg38UCSC Ensembl
OuterchrX:67878852..67910524hg38UCSC Ensembl
InnerchrX:67128508..67130144hg19UCSC Ensembl
OuterchrX:67098694..67130366hg19UCSC Ensembl
InnerchrX:67045233..67046869hg18UCSC Ensembl
OuterchrX:67015419..67047091hg18UCSC Ensembl
InnerchrX:66911529..66913165hg17UCSC Ensembl
OuterchrX:66881715..66913387hg17UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3831673
hg1931673
hg1831673
hg1731673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9950
Supporting Variants
SamplesNA19173
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)nssv26529
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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