A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483102



Internal ID15235576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42722031..42876093hg38UCSC Ensembl
Innerchr8:42577174..42731236hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38154063
hg19154063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996487
Samples
Known GenesCHRNA6, CHRNB3, RNF170, THAP1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483102
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer