A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526641



Internal ID15453934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3236606..3244721hg38UCSC Ensembl
Innerchr11:3257836..3265951hg19UCSC Ensembl
Innerchr11:3214412..3222527hg18UCSC Ensembl
Innerchr11:3214412..3222527hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388116
hg198116
hg188116
hg178116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702966
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526641
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer