A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9316



Internal ID15847228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:10001..32774hg38UCSC Ensembl
Outerchr16:60001..82774hg19UCSC Ensembl
Outerchr16:1..22774hg18UCSC Ensembl
Outerchr16:1..22774hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822774
hg1922774
hg1822774
hg1722774
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25615, nssv23262, nssv21894, nssv26510
SamplesNA18860, NA18975, NA18517, NA12740
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2
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)nsv9316
Frequency
Sample Size31
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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