A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513992



Internal ID18812273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101715747..101756108hg38UCSC Ensembl
Innerchr11:101586478..101626839hg19UCSC Ensembl
Innerchr11:101091688..101132049hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3840362
hg1940362
hg1840362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044223
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513992
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