A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066792



Internal ID20633832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22361801..22405600hg38UCSC Ensembl
chr20:22342439..22386238hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3843800
hg1943800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523241
Supporting Variants
Samples
Known GenesLOC284788
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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