A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482929



Internal ID15235658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58932626..59094208hg38UCSC Ensembl
Innerchr11:58700099..58861681hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38161583
hg19161583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996331
Samples
Known GenesGLYATL1, LOC283194
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482929
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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