A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469633



Internal ID15187662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31438800..31612410hg38UCSC Ensembl
Innerchr15:31731003..31904613hg19UCSC Ensembl
Innerchr15:29518295..29691905hg18UCSC Ensembl
Innerchr15:29447059..29620669hg16UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38173611
hg19173611
hg18173611
hg16173611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672668, nssv1674442, nssv1673105, nssv1673557, nssv1676445, nssv1673682, nssv1674418, nssv1676006, nssv1674012, nssv1676317
Samples
Known GenesOTUD7A
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)nsv469633
Frequency
Sample Size265
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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