A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24799



Internal ID15842309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90215678..90219517hg38UCSC Ensembl
Outerchr16:90200541..90225276hg38UCSC Ensembl
Innerchr16:90282086..90285925hg19UCSC Ensembl
Outerchr16:90266949..90291684hg19UCSC Ensembl
Innerchr16:88809587..88813426hg18UCSC Ensembl
Outerchr16:88794450..88819185hg18UCSC Ensembl
Innerchr16:88809587..88813426hg17UCSC Ensembl
Outerchr16:88794450..88819185hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3824736
hg1924736
hg1824736
hg1724736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9484
Supporting Variants
SamplesNA19144
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)nssv24799
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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