A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031362



Internal ID20598402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67514089..67527162hg38UCSC Ensembl
chr16:67547992..67561065hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3813074
hg1913074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501687
Supporting Variants
Samples
Known GenesLOC100505942
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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