A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22842



Internal ID15835876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29381919..29383569hg38UCSC Ensembl
Outerchr16:29381586..29384155hg38UCSC Ensembl
Innerchr16:29393240..29394890hg19UCSC Ensembl
Outerchr16:29392907..29395476hg19UCSC Ensembl
Innerchr16:29300741..29302391hg18UCSC Ensembl
Outerchr16:29300408..29302977hg18UCSC Ensembl
Innerchr16:29300741..29302391hg17UCSC Ensembl
Outerchr16:29300408..29302977hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382570
hg192570
hg182570
hg172570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9423
Supporting Variants
SamplesNA18563
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)nssv22842
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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