A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23400



Internal ID15481882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33792732..33830326hg38UCSC Ensembl
Outerchr16:33792173..33830514hg38UCSC Ensembl
Innerchr16:33595199..33632793hg19UCSC Ensembl
Outerchr16:33594640..33632981hg19UCSC Ensembl
Innerchr16:33502700..33540294hg18UCSC Ensembl
Outerchr16:33502141..33540482hg18UCSC Ensembl
Innerchr16:33502700..33540294hg17UCSC Ensembl
Outerchr16:33502141..33540482hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3838342
hg1938342
hg1838342
hg1738342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA10839
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)nssv23400
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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