A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27955



Internal ID15496953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32177734..32204896hg38UCSC Ensembl
Outerchr16:32175975..32205051hg38UCSC Ensembl
Innerchr16:32189055..32216217hg19UCSC Ensembl
Outerchr16:32187296..32216372hg19UCSC Ensembl
Innerchr16:32096556..32123718hg18UCSC Ensembl
Outerchr16:32094797..32123873hg18UCSC Ensembl
Innerchr16:32096556..32123718hg17UCSC Ensembl
Outerchr16:32094797..32123873hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3829077
hg1929077
hg1829077
hg1729077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19221
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)nssv27955
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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