A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26361



Internal ID15487610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32992675..32994691hg38UCSC Ensembl
Outerchr16:32992030..32995467hg38UCSC Ensembl
Innerchr16:33003996..33006012hg19UCSC Ensembl
Outerchr16:33003351..33006788hg19UCSC Ensembl
Innerchr16:32911497..32913513hg18UCSC Ensembl
Outerchr16:32910852..32914289hg18UCSC Ensembl
Innerchr16:32911497..32913513hg17UCSC Ensembl
Outerchr16:32910852..32914289hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383438
hg193438
hg183438
hg173438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18517
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)nssv26361
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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