A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528768



Internal ID15456061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115301341..115307333hg38UCSC Ensembl
Innerchr12:115739146..115745138hg19UCSC Ensembl
Innerchr12:114223529..114229521hg18UCSC Ensembl
Innerchr12:114201866..114207858hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg385993
hg195993
hg185993
hg175993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705432
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528768
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