A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519169



Internal ID15446462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56440110..56445633hg38UCSC Ensembl
Innerchr20:55015166..55020689hg19UCSC Ensembl
Innerchr20:54448573..54454096hg18UCSC Ensembl
Innerchr20:54448573..54454096hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385524
hg195524
hg185524
hg175524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv249n21
Supporting Variantsnssv696651
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519169
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