A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831952



Internal ID16109135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97238587..97386167hg38UCSC Ensembl
Outerchr10:98998344..99145924hg19UCSC Ensembl
Outerchr10:98988334..99135914hg18UCSC Ensembl
Outerchr10:98988334..99135914hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38147581
hg19147581
hg18147581
hg17147581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1448667, nssv1448666, nssv1448668, nssv1448669, nssv1448670
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1, FRAT1, FRAT2, RRP12
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)nsv831952
Frequency
Sample Size95
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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