A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672484



Internal ID15183306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:221682529..221866993hg38UCSC Ensembl
Innerchr1:221855871..222040335hg19UCSC Ensembl
Innerchr1:219922494..220106958hg18UCSC Ensembl
Innerchr1:218912162..219096626hg16UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38184465
hg19184465
hg18184465
hg16184465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469786
Supporting Variants
Samples
Known GenesDUSP10
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)nssv1672484
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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