A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23864



Internal ID15840904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90116842..90118499hg38UCSC Ensembl
Outerchr16:90116564..90118618hg38UCSC Ensembl
Innerchr16:90183250..90184907hg19UCSC Ensembl
Outerchr16:90182972..90185026hg19UCSC Ensembl
Innerchr16:88710751..88712408hg18UCSC Ensembl
Outerchr16:88710473..88712527hg18UCSC Ensembl
Innerchr16:88710751..88712408hg17UCSC Ensembl
Outerchr16:88710473..88712527hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382055
hg192055
hg182055
hg172055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9483
Supporting Variants
SamplesNA18980
Known Genes
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)nssv23864
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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