A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8367



Internal ID15499593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:92624381..92625979hg38UCSC Ensembl
Outerchr8:93636609..93638207hg19UCSC Ensembl
Outerchr8:93705785..93707383hg18UCSC Ensembl
Outerchr8:93705785..93707383hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
hg171599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17314
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)nsv8367
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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