A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243588



Internal ID20810628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66881671..66882440hg38UCSC Ensembl
chr16:66915574..66916343hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578457
Supporting Variants
Samples
Known GenesPDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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