A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16331



Internal ID15832263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69403728..69410301hg38UCSC Ensembl
Outerchr9:69402808..69410820hg38UCSC Ensembl
Innerchr9:72018644..72025217hg19UCSC Ensembl
Outerchr9:72017724..72025736hg19UCSC Ensembl
Innerchr9:71208464..71215037hg18UCSC Ensembl
Outerchr9:71207544..71215556hg18UCSC Ensembl
Innerchr9:69248198..69254771hg17UCSC Ensembl
Outerchr9:69247278..69255290hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg388013
hg198013
hg188013
hg178013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8522
Supporting Variants
SamplesNA12872
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)nssv16331
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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