A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239933



Internal ID20806973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14512237..14512939hg38UCSC Ensembl
chr16:14606094..14606796hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583847
Supporting Variants
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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