A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8456



Internal ID15846368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66930405..67305028hg38UCSC Ensembl
Outerchr9:40089166..40491719hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38374624
hg17402554
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18628, nssv17360, nssv20301, nssv18419, nssv18183, nssv22080, nssv17267, nssv15851, nssv18598, nssv18788, nssv16792, nssv22140, nssv17887, nssv19992, nssv18728, nssv16595, nssv20113, nssv20367, nssv19962
SamplesNA18502, NA11830, NA18504, NA12155, NA18563, NA18860, NA18942, NA07048, NA10847, NA12872, NA19221, NA18853, NA19132, NA19144, NA19173
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)nsv8456
Frequency
Sample Size31
Observed Gain3
Observed Loss13
Observed Complex0
Frequencyn/a


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