A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9481



Internal ID15500707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89900574..89902839hg38UCSC Ensembl
Outerchr16:89966982..89969247hg19UCSC Ensembl
Outerchr16:88494483..88496748hg18UCSC Ensembl
Outerchr16:88494483..88496748hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382266
hg192266
hg182266
hg172266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23313
SamplesNA07048
Known GenesTCF25
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)nsv9481
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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