A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1443321



Internal ID16093925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:197599786..197770453hg38UCSC Ensembl
Outerchr3:197326657..197497324hg19UCSC Ensembl
Outerchr3:198811054..198981721hg18UCSC Ensembl
Outerchr3:198814967..198985634hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38170668
hg19170668
hg18170668
hg17170668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv829831
Supporting Variants
Samples
Known GenesFYTTD1, KIAA0226, LOC220729, MIR922
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)nssv1443321
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