A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25545



Internal ID15487041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32741613..32741652hg38UCSC Ensembl
Outerchr16:32741562..32742111hg38UCSC Ensembl
Innerchr16:32752934..32752973hg19UCSC Ensembl
Outerchr16:32752883..32753432hg19UCSC Ensembl
Innerchr16:32660435..32660474hg18UCSC Ensembl
Outerchr16:32660384..32660933hg18UCSC Ensembl
Innerchr16:32660435..32660474hg17UCSC Ensembl
Outerchr16:32660384..32660933hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38550
hg19550
hg18550
hg17550
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)nssv25545
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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