A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511986



Internal ID18810267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5772341..5787806hg38UCSC Ensembl
Innerchr11:5793571..5809036hg19UCSC Ensembl
Innerchr11:5750147..5765612hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815466
hg1915466
hg1815466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048420
Supporting Variants
Samples
Known GenesOR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511986
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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