A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469698



Internal ID15534413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194772104..194937813hg38UCSC Ensembl
Innerchr3:194492833..194658542hg19UCSC Ensembl
Innerchr3:195974122..196139831hg18UCSC Ensembl
Innerchr3:195812341..195978050hg16UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38165710
hg19165710
hg18165710
hg16165710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672787, nssv1674830, nssv1673190
Samples
Known GenesLOC100507391
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469698
Frequency
Sample Size265
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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