A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244337



Internal ID20811377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69389234..69389722hg38UCSC Ensembl
chr16:69423137..69423625hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244337
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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