A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517697



Internal ID20891058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18526038..18534802hg38UCSC Ensembl
chr20:18506682..18515446hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388765
hg198765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205251
Samples
Known GenesSEC23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517697
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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