A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069204



Internal ID20636244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60377884..60383531hg38UCSC Ensembl
chr20:58952942..58958589hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385648
hg195648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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