A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24069



Internal ID15484758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86496978..86497583hg38UCSC Ensembl
Outerchr16:86496320..86498276hg38UCSC Ensembl
Innerchr16:86530584..86531189hg19UCSC Ensembl
Outerchr16:86529926..86531882hg19UCSC Ensembl
Innerchr16:85088085..85088690hg18UCSC Ensembl
Outerchr16:85087427..85089383hg18UCSC Ensembl
Innerchr16:85088085..85088690hg17UCSC Ensembl
Outerchr16:85087427..85089383hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381957
hg191957
hg181957
hg171957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9468
Supporting Variants
SamplesNA12740
Known GenesFENDRR
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)nssv24069
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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