A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028907



Internal ID20595947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22915969..22928738hg38UCSC Ensembl
chr16:22927290..22940059hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3812770
hg1912770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496698
Supporting Variants
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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