A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23410



Internal ID15488793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33624595..33696012hg38UCSC Ensembl
Outerchr16:33623544..33696701hg38UCSC Ensembl
Innerchr16:33427062..33498479hg19UCSC Ensembl
Outerchr16:33426011..33499168hg19UCSC Ensembl
Innerchr16:33334563..33405980hg18UCSC Ensembl
Outerchr16:33333512..33406669hg18UCSC Ensembl
Innerchr16:33334563..33405980hg17UCSC Ensembl
Outerchr16:33333512..33406669hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3873158
hg1973158
hg1873158
hg1773158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18552
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)nssv23410
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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