A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469632



Internal ID15187661
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672384, nssv1676348, nssv1672085, nssv1672209, nssv1676032, nssv1675034
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)nsv469632
Frequency
Sample Size265
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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