A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483119



Internal ID15582232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:72849120..72991218hg38UCSC Ensembl
Innerchr18:70516355..70658453hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38142099
hg19142099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996366
Samples
Known GenesNETO1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483119
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