A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830793



Internal ID16454662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:99530269..99699083hg38UCSC Ensembl
Outerchr1:99995825..100164639hg19UCSC Ensembl
Outerchr1:99768413..99937227hg18UCSC Ensembl
Outerchr1:99707846..99876660hg17UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38168815
hg19168815
hg18168815
hg17168815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1448150, nssv1448161, nssv1448185, nssv1448196, nssv1448139, nssv1448172
Samples
Known GenesMIR548AA1, MIR548D1, PALMD
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)nsv830793
Frequency
Sample Size95
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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