A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831084



Internal ID16108267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:103138461..103324523hg38UCSC Ensembl
Outerchr7:102778908..102964970hg19UCSC Ensembl
Outerchr7:102566144..102752206hg18UCSC Ensembl
Outerchr7:102372859..102558921hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38186063
hg19186063
hg18186063
hg17186063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1446378, nssv1446377
Samples
Known GenesDNAJC2, DPY19L2P2, NAPEPLD, PMPCB, RPL19P12
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)nsv831084
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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