A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686440



Internal ID15076406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11992266..11993709hg38UCSC Ensembl
Innerchr11:12013813..12015256hg19UCSC Ensembl
Innerchr11:11970389..11971832hg18UCSC Ensembl
Innerchr11:11970389..11971832hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381444
hg191444
hg181444
hg171444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515847
Supporting Variants
Samples
Known GenesDKK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686440
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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