A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986



Internal ID15835287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40298061..40322168hg38UCSC Ensembl
Outerchr9:40293928..40324770hg38UCSC Ensembl
Innerchr9:43034715..43058824hg19UCSC Ensembl
Outerchr9:43032113..43062956hg19UCSC Ensembl
Innerchr9:43024711..43048820hg18UCSC Ensembl
Outerchr9:43022109..43052952hg18UCSC Ensembl
Innerchr9:45593357..45617464hg17UCSC Ensembl
Outerchr9:45589224..45620066hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3830843
hg1930844
hg1830844
hg1730843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8486
Supporting Variants
SamplesNA18552
Known GenesFAM95B1
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)nssv17986
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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