A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1447761



Internal ID16098365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61863001..61949740hg38UCSC Ensembl
Outerchr9:46116776..46206932hg19UCSC Ensembl
Outerchr9:46006772..46096928hg18UCSC Ensembl
Outerchr9:44669521..44759677hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3886740
hg1990157
hg1890157
hg1790157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv831587
Supporting Variants
Samples
Known Genes
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)nssv1447761
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer