A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066287



Internal ID20633327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11098082..11098609hg38UCSC Ensembl
chr20:11078730..11079257hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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