A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527645



Internal ID15454938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:12502954..12578874hg38UCSC Ensembl
Innerchr20:12483602..12559521hg19UCSC Ensembl
Innerchr20:12431602..12507521hg18UCSC Ensembl
Innerchr20:12431602..12507521hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3875921
hg1975920
hg1875920
hg1775920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704116
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527645
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