A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469626



Internal ID15187655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15599642..15766452hg38UCSC Ensembl
Innerchr16:15693499..15860309hg19UCSC Ensembl
Innerchr16:15601000..15767810hg18UCSC Ensembl
Innerchr16:15659938..15826748hg16UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38166811
hg19166811
hg18166811
hg16166811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675802, nssv1675752, nssv1675057
Samples
Known GenesKIAA0430, MIR484, MIR6506, MYH11, NDE1
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)nsv469626
Frequency
Sample Size265
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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