A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469702



Internal ID15187731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23401453..23548569hg38UCSC Ensembl
Innerchr22:23743640..23890756hg19UCSC Ensembl
Innerchr22:22073640..22220756hg18UCSC Ensembl
Innerchr22:22068194..22215310hg16UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38147117
hg19147117
hg18147117
hg16147117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675462
Samples
Known GenesZDHHC8P1
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)nsv469702
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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