A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525626



Internal ID15106233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3475112..3535277hg38UCSC Ensembl
Innerchr20:3455759..3515924hg19UCSC Ensembl
Innerchr20:3403759..3463924hg18UCSC Ensembl
Innerchr20:3403759..3463924hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3860166
hg1960166
hg1860166
hg1760166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701775
Samples
Known GenesATRN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525626
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