A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833731



Internal ID16110914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7589114..7739331hg38UCSC Ensembl
Outerchr19:7654000..7804217hg19UCSC Ensembl
Outerchr19:7560000..7710217hg18UCSC Ensembl
Outerchr19:7560000..7710217hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38150218
hg19150218
hg18150218
hg17150218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1454295, nssv1454294
Samples
Known GenesC19orf59, CAMSAP3, CLEC4G, FCER2, MIR6792, PCP2, PET100, RETN, STXBP2, TRAPPC5, XAB2
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)nsv833731
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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