A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26510



Internal ID15838169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13362..19494hg38UCSC Ensembl
Outerchr16:10001..23304hg38UCSC Ensembl
Innerchr16:63362..69494hg19UCSC Ensembl
Outerchr16:60001..73304hg19UCSC Ensembl
Innerchr16:3362..9494hg18UCSC Ensembl
Outerchr16:1..13304hg18UCSC Ensembl
Innerchr16:3362..9494hg17UCSC Ensembl
Outerchr16:1..13304hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813304
hg1913304
hg1813304
hg1713304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9316
Supporting Variants
SamplesNA18860
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)nssv26510
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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