A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242680



Internal ID20809720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23540953..23541734hg38UCSC Ensembl
chr16:23552274..23553055hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582674
Supporting Variants
Samples
Known GenesEARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242680
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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