A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240862



Internal ID20807902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84148611..84149472hg38UCSC Ensembl
chr16:84182216..84183077hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591495
Supporting Variants
Samples
Known GenesDNAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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