A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673300



Internal ID15184122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144842323..145040108hg38UCSC Ensembl
Innerchr8:146067708..146265494hg19UCSC Ensembl
Innerchr8:146038512..146236298hg18UCSC Ensembl
Innerchr8:146072505..146270291hg16UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38197786
hg19197787
hg18197787
hg16197787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469809
Supporting Variants
Samples
Known GenesCOMMD5, TMED10P1, ZNF16, ZNF250, ZNF252P, ZNF252P-AS1, ZNF7
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)nssv1673300
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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