A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520725



Internal ID6016161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23731386..23917281hg19UCSC Ensembl
Innerchr13:22629386..22815281hg18UCSC Ensembl
Innerchr13:22629386..22815281hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv697577
Samples
Known GenesSACS, SGCG
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv520725
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