A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469586



Internal ID15187615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313349..30491181hg38UCSC Ensembl
Innerchr15:30605552..30783384hg19UCSC Ensembl
Innerchr15:28392844..28570676hg18UCSC Ensembl
Innerchr15:28321608..28499440hg16UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38177833
hg19177833
hg18177833
hg16177833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672196, nssv1676702, nssv1673040, nssv1674514, nssv1674662, nssv1672907
Samples
Known GenesCHRFAM7A, LOC101059918
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)nsv469586
Frequency
Sample Size265
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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