A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26513



Internal ID15495037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70191905..70196727hg38UCSC Ensembl
Outerchr16:70190772..70196741hg38UCSC Ensembl
Innerchr16:70225808..70230630hg19UCSC Ensembl
Outerchr16:70224675..70230644hg19UCSC Ensembl
Innerchr16:68783309..68788131hg18UCSC Ensembl
Outerchr16:68782176..68788145hg18UCSC Ensembl
Innerchr16:68783309..68788131hg17UCSC Ensembl
Outerchr16:68782176..68788145hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385970
hg195970
hg185970
hg175970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA19132
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)nssv26513
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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