A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469726



Internal ID15534441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32133693..32332547hg38UCSC Ensembl
Innerchr15:32425894..32624748hg19UCSC Ensembl
Innerchr15:30213186..30412040hg18UCSC Ensembl
Innerchr15:30141950..30340804hg16UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38198855
hg19198855
hg18198855
hg16198855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675190, nssv1675575, nssv1675718, nssv1674402, nssv1676015, nssv1674095, nssv1673938, nssv1676513, nssv1672967, nssv1673836, nssv1672450, nssv1673044, nssv1675288, nssv1675478, nssv1673972, nssv1675409, nssv1675847, nssv1673459, nssv1674581, nssv1674942
Samples
Known GenesCHRNA7
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)nsv469726
Frequency
Sample Size265
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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