A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667420



Internal ID15057386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130155050..130204295hg38UCSC Ensembl
Innerchr11:130024945..130074190hg19UCSC Ensembl
Innerchr11:129530155..129579400hg18UCSC Ensembl
Innerchr11:129530155..129579400hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3849246
hg1949246
hg1849246
hg1749246
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517199
Supporting Variants
Samples
Known GenesST14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667420
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