A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469835



Internal ID15534550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2824136..3005987hg38UCSC Ensembl
Innerchr1:2740701..2922551hg19UCSC Ensembl
Innerchr1:2730561..2912411hg18UCSC Ensembl
Innerchr1:2523684..2705534hg16UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38181852
hg19181851
hg18181851
hg16181851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675009
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)nsv469835
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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