A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8471



Internal ID15499697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67704932..67742186hg38UCSC Ensembl
Outerchr9:44974795..45012050hg19UCSC Ensembl
Outerchr9:44914791..44952046hg18UCSC Ensembl
Outerchr9:44185383..44222638hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3837255
hg1937256
hg1837256
hg1737256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21147, nssv22560
SamplesNA19221, NA19132
Known GenesFAM27C
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)nsv8471
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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