A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23507



Internal ID15496690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16291538..16291580hg38UCSC Ensembl
Outerchr16:16291092..16292215hg38UCSC Ensembl
Innerchr16:16385395..16385437hg19UCSC Ensembl
Outerchr16:16384949..16386072hg19UCSC Ensembl
Innerchr16:16292896..16292938hg18UCSC Ensembl
Outerchr16:16292450..16293573hg18UCSC Ensembl
Innerchr16:16292896..16292938hg17UCSC Ensembl
Outerchr16:16292450..16293573hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
hg171124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9362
Supporting Variants
SamplesNA19173
Known GenesNOMO3
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)nssv23507
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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