A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523057



Internal ID15103664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45152979..45160131hg38UCSC Ensembl
Innerchr11:45174530..45181682hg19UCSC Ensembl
Innerchr11:45131106..45138258hg18UCSC Ensembl
Innerchr11:45131106..45138258hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387153
hg197153
hg187153
hg177153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698740
Samples
Known GenesPRDM11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523057
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