A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18809



Internal ID15496302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81596031..81597295hg38UCSC Ensembl
Outerchr9:81595391..81597685hg38UCSC Ensembl
Innerchr9:84210946..84212210hg19UCSC Ensembl
Outerchr9:84210306..84212600hg19UCSC Ensembl
Innerchr9:83400766..83402030hg18UCSC Ensembl
Outerchr9:83400126..83402420hg18UCSC Ensembl
Innerchr9:81440500..81441764hg17UCSC Ensembl
Outerchr9:81439860..81442154hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382295
hg192295
hg182295
hg172295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8532
Supporting Variants
SamplesNA19173
Known GenesTLE1
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)nssv18809
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