A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665005



Internal ID15054971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11992070..11994183hg38UCSC Ensembl
Innerchr11:12013617..12015730hg19UCSC Ensembl
Innerchr11:11970193..11972306hg18UCSC Ensembl
Innerchr11:11970193..11972306hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382114
hg192114
hg182114
hg172114
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)nssv665005
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