A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8586



Internal ID15846498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137449953..137452560hg38UCSC Ensembl
Outerchr9:140344405..140347012hg19UCSC Ensembl
Outerchr9:139464226..139466833hg18UCSC Ensembl
Outerchr9:137620242..137622849hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382608
hg192608
hg182608
hg172608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23254
SamplesNA19221
Known GenesMIR7114, NSMF
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)nsv8586
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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