A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10n29



Internal ID20133227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26873304..27047819hg38UCSC Ensembl
chr6:26841083..27015598hg19UCSC Ensembl
chr6:26949062..27123577hg18UCSC Ensembl
chr6:26949062..27123577hg16UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38174516
hg19174516
hg18174516
hg16174516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv469675, nsv469610
Samples
Known GenesGUSBP2, LINC00240, LOC100270746
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)dgv10n29
Frequency
Sample Size265
Observed Gain45
Observed Loss0
Observed Complex0
Frequencyn/a


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