A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520545



Internal ID15447838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10891422..10891662hg38UCSC Ensembl
Innerchr2:11031548..11031788hg19UCSC Ensembl
Innerchr2:10948999..10949239hg18UCSC Ensembl
Innerchr2:10982146..10982386hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
hg17241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697478
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520545
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