A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031787



Internal ID20598827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69387533..69388009hg38UCSC Ensembl
chr16:69421436..69421912hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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