A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519787



Internal ID20893148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23866112..23963325hg38UCSC Ensembl
chr20:23846749..23943962hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3897214
hg1997214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066879
Samples
Known GenesCST5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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