A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671871



Internal ID15061837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17556667..17577072hg38UCSC Ensembl
Innerchr20:17537312..17557717hg19UCSC Ensembl
Innerchr20:17485312..17505717hg18UCSC Ensembl
Innerchr20:17485312..17505717hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3820406
hg1920406
hg1820406
hg1720406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520496
Supporting Variants
Samples
Known GenesBFSP1, DSTN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671871
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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