A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469546



Internal ID15534261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153984700..154186715hg38UCSC Ensembl
Innerchr7:153681785..153883800hg19UCSC Ensembl
Innerchr7:153312718..153514733hg18UCSC Ensembl
Innerchr7:153073525..153275540hg16UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38202016
hg19202016
hg18202016
hg16202016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675591
Samples
Known GenesDPP6
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)nsv469546
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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