A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520010



Internal ID15100617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124958039..125065461hg38UCSC Ensembl
Innerchr11:124827935..124935357hg19UCSC Ensembl
Innerchr11:124333145..124440567hg18UCSC Ensembl
Innerchr11:124333145..124440567hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38107423
hg19107423
hg18107423
hg17107423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663232, nssv681477, nssv660074
Samples
Known GenesCCDC15, SLC37A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520010
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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