A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18309



Internal ID15831183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38868382..38874542hg38UCSC Ensembl
Outerchr9:38859978..38875116hg38UCSC Ensembl
Innerchr9:38868379..38874539hg19UCSC Ensembl
Outerchr9:38859975..38875113hg19UCSC Ensembl
Innerchr9:38858379..38864539hg18UCSC Ensembl
Outerchr9:38849975..38865113hg18UCSC Ensembl
Innerchr9:38858379..38864539hg17UCSC Ensembl
Outerchr9:38849975..38865113hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3815139
hg1915139
hg1815139
hg1715139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA12740
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)nssv18309
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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