A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18418



Internal ID15495803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39316012..39333221hg38UCSC Ensembl
Outerchr9:39314103..39336451hg38UCSC Ensembl
Innerchr9:39316009..39333218hg19UCSC Ensembl
Outerchr9:39314100..39336448hg19UCSC Ensembl
Innerchr9:39306009..39323218hg18UCSC Ensembl
Outerchr9:39304100..39326448hg18UCSC Ensembl
Innerchr9:39306009..39323218hg17UCSC Ensembl
Outerchr9:39304100..39326448hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3822349
hg1922349
hg1822349
hg1722349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8450
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)nssv18418
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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