A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21382



Internal ID15492207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32688777..32693750hg38UCSC Ensembl
Outerchr16:32687905..32693986hg38UCSC Ensembl
Innerchr16:32700098..32705071hg19UCSC Ensembl
Outerchr16:32699226..32705307hg19UCSC Ensembl
Innerchr16:32607599..32612572hg18UCSC Ensembl
Outerchr16:32606727..32612808hg18UCSC Ensembl
Innerchr16:32607599..32612572hg17UCSC Ensembl
Outerchr16:32606727..32612808hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386082
hg196082
hg186082
hg176082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18942
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)nssv21382
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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