A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526184



Internal ID15453477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:65721421..65737283hg38UCSC Ensembl
Innerchr12:66115201..66131063hg19UCSC Ensembl
Innerchr12:64401468..64417330hg18UCSC Ensembl
Innerchr12:64401468..64417330hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3815863
hg1915863
hg1815863
hg1715863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv97n21
Supporting Variantsnssv702446
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526184
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