A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519542



Internal ID15446835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17610934..17648517hg38UCSC Ensembl
Innerchr20:17591579..17629162hg19UCSC Ensembl
Innerchr20:17539579..17577162hg18UCSC Ensembl
Innerchr20:17539579..17577162hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3837584
hg1937584
hg1837584
hg1737584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661150, nssv672595, nssv656786, nssv680974, nssv694015, nssv660439, nssv679781
Samples
Known GenesRRBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519542
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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