A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528221



Internal ID15455514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22752111..22786642hg38UCSC Ensembl
Innerchr20:22732749..22767280hg19UCSC Ensembl
Innerchr20:22680749..22715280hg18UCSC Ensembl
Innerchr20:22680749..22715280hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3834532
hg1934532
hg1834532
hg1734532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704782
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528221
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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