A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9326



Internal ID15500552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:856661..867235hg38UCSC Ensembl
Outerchr16:906661..917235hg19UCSC Ensembl
Outerchr16:846662..857236hg18UCSC Ensembl
Outerchr16:846662..857236hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810575
hg1910575
hg1810575
hg1710575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24941, nssv26582, nssv23253
SamplesNA18504, NA18860, NA19173
Known GenesLMF1
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)nsv9326
Frequency
Sample Size31
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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