A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520016



Internal ID15447309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41669142..41672041hg38UCSC Ensembl
Innerchr21:43089302..43092201hg19UCSC Ensembl
Innerchr21:41962371..41965270hg18UCSC Ensembl
Innerchr21:41962371..41965270hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382900
hg192900
hg182900
hg172900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687776, nssv660093
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520016
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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