A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518276



Internal ID20891637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24215201..24224700hg38UCSC Ensembl
chr20:24195837..24205336hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203243
Samples
Known GenesFLJ33581
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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