A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18358



Internal ID15842492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38868382..38873938hg38UCSC Ensembl
Outerchr9:38859978..38874436hg38UCSC Ensembl
Innerchr9:38868379..38873935hg19UCSC Ensembl
Outerchr9:38859975..38874433hg19UCSC Ensembl
Innerchr9:38858379..38863935hg18UCSC Ensembl
Outerchr9:38849975..38864433hg18UCSC Ensembl
Innerchr9:38858379..38863935hg17UCSC Ensembl
Outerchr9:38849975..38864433hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3814459
hg1914459
hg1814459
hg1714459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA19144
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)nssv18358
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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