A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521545



Internal ID15448838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28743577..28762477hg38UCSC Ensembl
Innerchr21:30115899..30134799hg19UCSC Ensembl
Innerchr21:29037770..29056670hg18UCSC Ensembl
Innerchr21:29037770..29056670hg17UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3818901
hg1918901
hg1818901
hg1718901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698161
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521545
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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