A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514166



Internal ID18812447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107678441..107752052hg38UCSC Ensembl
Innerchr11:107549167..107622778hg19UCSC Ensembl
Innerchr11:107054377..107127988hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3873612
hg1973612
hg1873612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045492
Supporting Variants
Samples
Known GenesSLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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