A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469526



Internal ID15534241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39548632hg38UCSC Ensembl
Innerchr9:41574131..41693650hg19UCSC Ensembl
Innerchr9:41564131..41683650hg18UCSC Ensembl
Innerchr9:40465770..40585289hg16UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38103132
hg19119520
hg18119520
hg16119520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672544, nssv1675148, nssv1672419
Samples
Known GenesLOC653501, ZNF658B
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)nsv469526
Frequency
Sample Size265
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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