A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674908



Internal ID15185730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22720659..22890398hg38UCSC Ensembl
Innerchr15:22982670..23152437hg19UCSC Ensembl
Innerchr15:20534111..20703878hg18UCSC Ensembl
Innerchr15:20530379..20700146hg16UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38169740
hg19169768
hg18169768
hg16169768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469667
Supporting Variants
Samples
Known GenesCYFIP1, LOC283683, NIPA1, NIPA2
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)nssv1674908
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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