A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23710



Internal ID15481910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70116870..70163861hg38UCSC Ensembl
Outerchr16:70114032..70164492hg38UCSC Ensembl
Innerchr16:70150773..70197764hg19UCSC Ensembl
Outerchr16:70147935..70198395hg19UCSC Ensembl
Innerchr16:68708274..68755265hg18UCSC Ensembl
Outerchr16:68705436..68755896hg18UCSC Ensembl
Innerchr16:68708274..68755265hg17UCSC Ensembl
Outerchr16:68705436..68755896hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3850461
hg1950461
hg1850461
hg1750461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA10839
Known GenesPDPR
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)nssv23710
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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