A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26644



Internal ID15486248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33803073..33816580hg38UCSC Ensembl
Outerchr16:33801970..33817181hg38UCSC Ensembl
Innerchr16:33605540..33619047hg19UCSC Ensembl
Outerchr16:33604437..33619648hg19UCSC Ensembl
Innerchr16:33513041..33526548hg18UCSC Ensembl
Outerchr16:33511938..33527149hg18UCSC Ensembl
Innerchr16:33513041..33526548hg17UCSC Ensembl
Outerchr16:33511938..33527149hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815212
hg1915212
hg1815212
hg1715212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18502
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)nssv26644
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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