A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23521



Internal ID15488084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33493431..33521550hg38UCSC Ensembl
Outerchr16:33389099..33523952hg38UCSC Ensembl
Innerchr16:33295898..33324017hg19UCSC Ensembl
Outerchr16:33290340..33326419hg19UCSC Ensembl
Innerchr16:33203399..33231518hg18UCSC Ensembl
Outerchr16:33197841..33233920hg18UCSC Ensembl
Innerchr16:33203399..33231518hg17UCSC Ensembl
Outerchr16:33197841..33233920hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38134854
hg1936080
hg1836080
hg1736080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18537
Known GenesLOC390705
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)nssv23521
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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