A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672384



Internal ID15529892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39247033..39397767hg38UCSC Ensembl
Innerchr9:39247030..39397764hg19UCSC Ensembl
Innerchr9:39237030..39387764hg18UCSC Ensembl
Innerchr9:39237030..39387764hg16UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38150735
hg19150735
hg18150735
hg16150735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469632
Supporting Variants
Samples
Known GenesCNTNAP3, SPATA31A1, SPATA31A2
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)nssv1672384
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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