A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1455071



Internal ID16105675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:36477427..36658869hg38UCSC Ensembl
Outerchr20:35105830..35287272hg19UCSC Ensembl
Outerchr20:34539244..34720686hg18UCSC Ensembl
Outerchr20:34539244..34720686hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38181443
hg19181443
hg18181443
hg17181443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv833967
Supporting Variants
Samples
Known GenesC20orf24, DLGAP4, MYL9, NDRG3, SLA2, TGIF2, TGIF2-C20orf24
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)nssv1455071
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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