A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241437



Internal ID20808477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74971451..74972806hg38UCSC Ensembl
chr16:75005349..75006704hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381356
hg191356
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589697
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241437
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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