A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700154



Internal ID15090120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11964514..11966895hg38UCSC Ensembl
Innerchr11:11986061..11988442hg19UCSC Ensembl
Innerchr11:11942637..11945018hg18UCSC Ensembl
Innerchr11:11942637..11945018hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382382
hg192382
hg182382
hg172382
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524257
Supporting Variants
Samples
Known GenesDKK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700154
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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