A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1450662



Internal ID16101266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:153433366..153603667hg38UCSC Ensembl
Outerchr1:153405842..153576143hg19UCSC Ensembl
Outerchr1:151672466..151842767hg18UCSC Ensembl
Outerchr1:150218915..150389216hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38170302
hg19170302
hg18170302
hg17170302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv831603
Supporting Variants
Samples
Known GenesS100A2, S100A3, S100A4, S100A5, S100A6, S100A7, S100A7L2
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)nssv1450662
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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