A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518843



Internal ID15446136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19118391..19121053hg38UCSC Ensembl
Innerchr20:19099035..19101697hg19UCSC Ensembl
Innerchr20:19047035..19049697hg18UCSC Ensembl
Innerchr20:19047035..19049697hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382663
hg192663
hg182663
hg172663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696297
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518843
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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