A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21537



Internal ID15841713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138145219..138240223hg38UCSC Ensembl
Outerchr9:138144921..138240699hg38UCSC Ensembl
Innerchr9:141039671..141130673hg19UCSC Ensembl
Outerchr9:141039373..141131149hg19UCSC Ensembl
Innerchr9:140159492..140250494hg18UCSC Ensembl
Outerchr9:140159194..140250970hg18UCSC Ensembl
Innerchr9:138315508..138406510hg17UCSC Ensembl
Outerchr9:138315210..138406986hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3895779
hg1991777
hg1891777
hg1791777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8590
Supporting Variants
SamplesNA19132
Known GenesFAM157B, TUBBP5
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)nssv21537
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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