A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686409



Internal ID15423061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:66363293..66370085hg38UCSC Ensembl
Innerchr5:65659121..65665913hg19UCSC Ensembl
Innerchr5:65694877..65701669hg18UCSC Ensembl
Innerchr5:65694877..65701669hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg386793
hg196793
hg186793
hg176793
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520876
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686409
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