A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469631



Internal ID15534346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67413327..67571354hg38UCSC Ensembl
Innerchr7:66878314..67036341hg19UCSC Ensembl
Innerchr7:66515749..66673776hg18UCSC Ensembl
Innerchr7:66289930..66447957hg16UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38158028
hg19158028
hg18158028
hg16158028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673707, nssv1676471
Samples
Known Genes
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)nsv469631
Frequency
Sample Size265
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer