A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9472



Internal ID15500698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87986404..87994114hg38UCSC Ensembl
Outerchr16:88020010..88027720hg19UCSC Ensembl
Outerchr16:86577511..86585221hg18UCSC Ensembl
Outerchr16:86577511..86585221hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg387711
hg197711
hg187711
hg177711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26780
SamplesNA18502
Known GenesBANP
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)nsv9472
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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