A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663235



Internal ID15399887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63070597..63080090hg38UCSC Ensembl
Innerchr11:62838069..62847562hg19UCSC Ensembl
Innerchr11:62594645..62604138hg18UCSC Ensembl
Innerchr11:62594645..62604138hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg389494
hg199494
hg189494
hg179494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517447
Supporting Variants
Samples
Known GenesSLC22A24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663235
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