A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526898



Internal ID15107505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106013358..106022767hg38UCSC Ensembl
Innerchr11:105884085..105893494hg19UCSC Ensembl
Innerchr11:105389295..105398704hg18UCSC Ensembl
Innerchr11:105389295..105398704hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389410
hg199410
hg189410
hg179410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv81n21
Supporting Variantsnssv703257
Samples
Known GenesMSANTD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526898
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