A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672945



Internal ID15530453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20381603..20587625hg38UCSC Ensembl
Innerchr8:20239114..20445136hg19UCSC Ensembl
Innerchr8:20283394..20489416hg18UCSC Ensembl
Innerchr8:20249387..20455409hg16UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38206023
hg19206023
hg18206023
hg16206023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469890
Supporting Variants
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)nssv1672945
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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