A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25396



Internal ID15486993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32179606..32180105hg38UCSC Ensembl
Outerchr16:32178991..32180509hg38UCSC Ensembl
Innerchr16:32190927..32191426hg19UCSC Ensembl
Outerchr16:32190312..32191830hg19UCSC Ensembl
Innerchr16:32098428..32098927hg18UCSC Ensembl
Outerchr16:32097813..32099331hg18UCSC Ensembl
Innerchr16:32098428..32098927hg17UCSC Ensembl
Outerchr16:32097813..32099331hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381519
hg191519
hg181519
hg171519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18504
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)nssv25396
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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