A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8411



Internal ID15846323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:7420218..7450456hg38UCSC Ensembl
Outerchr9:7420218..7450456hg19UCSC Ensembl
Outerchr9:7410218..7440456hg18UCSC Ensembl
Outerchr9:7410218..7440456hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3830239
hg1930239
hg1830239
hg1730239
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19542, nssv17898
SamplesNA18502, NA18564
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)nsv8411
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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