A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24438



Internal ID15484087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32848634..32848754hg38UCSC Ensembl
Outerchr16:32848344..32849502hg38UCSC Ensembl
Innerchr16:32859955..32860075hg19UCSC Ensembl
Outerchr16:32859665..32860823hg19UCSC Ensembl
Innerchr16:32767456..32767576hg18UCSC Ensembl
Outerchr16:32767166..32768324hg18UCSC Ensembl
Innerchr16:32767456..32767576hg17UCSC Ensembl
Outerchr16:32767166..32768324hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381159
hg191159
hg181159
hg171159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA12155
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)nssv24438
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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