A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24680



Internal ID15483987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33626685..33687204hg38UCSC Ensembl
Outerchr16:33626356..33687527hg38UCSC Ensembl
Innerchr16:33429152..33489671hg19UCSC Ensembl
Outerchr16:33428823..33489994hg19UCSC Ensembl
Innerchr16:33336653..33397172hg18UCSC Ensembl
Outerchr16:33336324..33397495hg18UCSC Ensembl
Innerchr16:33336653..33397172hg17UCSC Ensembl
Outerchr16:33336324..33397495hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3861172
hg1961172
hg1861172
hg1761172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA12155
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)nssv24680
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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