A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482998



Internal ID15582366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84958665..85128740hg38UCSC Ensembl
Innerchr11:84669709..84839784hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38170076
hg19170076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996467, nssv2996241
Samples
Known GenesDLG2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482998
Frequency
Sample Size39
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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