A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831226



Internal ID16108409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:119788976..119980845hg38UCSC Ensembl
Outerchr1:120331599..120523468hg19UCSC Ensembl
Outerchr1:120133122..120324991hg18UCSC Ensembl
Outerchr1:120043641..120235510hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38191870
hg19191870
hg18191870
hg17191870
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449228, nssv1449217
Samples
Known GenesADAM30, NBPF7, NOTCH2, REG4
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)nsv831226
Frequency
Sample Size95
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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