A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831757



Internal ID16108940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135885814..136184089hg38UCSC Ensembl
Outerchr9:138777660..139075935hg19UCSC Ensembl
Outerchr9:137917481..138215756hg18UCSC Ensembl
Outerchr9:136003605..136301880hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38298276
hg19298276
hg18298276
hg17298276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1448136, nssv1448135, nssv1448137, nssv1448133, nssv1448132, nssv1448134, nssv1448131
Samples
Known GenesC9orf69, CAMSAP1, NACC2, UBAC1
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831757
Frequency
Sample Size95
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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