A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520095



Internal ID15447388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4967602..4990075hg38UCSC Ensembl
Innerchr20:4948248..4970721hg19UCSC Ensembl
Innerchr20:4896248..4918721hg18UCSC Ensembl
Innerchr20:4896248..4918721hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822474
hg1922474
hg1822474
hg1722474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660675, nssv684678
Samples
Known GenesSLC23A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520095
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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