A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25237



Internal ID15498009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33570427..33682094hg38UCSC Ensembl
Outerchr16:33569467..33683348hg38UCSC Ensembl
Innerchr16:33372894..33484561hg19UCSC Ensembl
Outerchr16:33371934..33485815hg19UCSC Ensembl
Innerchr16:33280395..33392062hg18UCSC Ensembl
Outerchr16:33279435..33393316hg18UCSC Ensembl
Innerchr16:33280395..33392062hg17UCSC Ensembl
Outerchr16:33279435..33393316hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38113882
hg19113882
hg18113882
hg17113882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19240
Known GenesRNU6-76P
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)nssv25237
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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