A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673231



Internal ID15184053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28093860..28252180hg38UCSC Ensembl
Innerchr16:28105181..28263501hg19UCSC Ensembl
Innerchr16:28012682..28171002hg18UCSC Ensembl
Innerchr16:28071585..28229969hg16UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38158321
hg19158321
hg18158321
hg16158385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469663
Supporting Variants
Samples
Known GenesXPO6
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)nssv1673231
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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